ANNEX III: MALE CONDOM INSPECTION, SAMPLING AND TESTING SPECIFICATIONS

Similar documents
ANNEX III: CONDOM TESTING SPECIFICATIONS

SECTION VIII: ANNEX D: MALE CONDOM INSPECTION, SAMPLING AND TESTING SPECIFICATIONS PRE-SHIPMENT TESTING

SECTION VIII: ANNEX A- FEMALE CONDOM INSPECTION, SAMPLING AND TESTING SPECIFICATIONS PREQUALIFICATION TESTING

THIS IS UNFPA. Male Latex Condom Testing Guidance UNICEF UNFPA WHO Joint Meeting September David Hill

WHO/UNFPA Specification for Male Latex Condoms

INTERNATIONAL STANDARD

ISO INTERNATIONAL STANDARD. Male condoms Requirements and test methods for condoms made from synthetic materials

Provläsningsexemplar / Preview INTERNATIONAL STANDARD. Rubber condoms - Part 1: Requirements

LUBRICANT, WATER BASED, NON-IRRITANT, FOR USE DURING INTERCOURSE

Kondomer av naturgummilatex för män Natural rubber latex male condoms

LIQUID PENETRANT EXAMINATION PROCEDURE

Quality Analysis of Male Latex Condoms Available in Private and Public Facilities in Lusaka, Zambia A Comparative Study

Fortified Refined Cottonseed Oil -COTTONSEED OIL-

helping you make the right choices

Fortified Refined Soybean Oil -SOYBEAN OIL-

CHEMISTRY CHANGES EVERYTHING

ISO 1567 INTERNATIONAL STANDARD. Dentistry Denture base polymers. Art dentaire Polymères pour base de prothèses dentaires. Third edition

Cardinal Health Cleanroom Gloves. Advancing performance by design

Engineering Materials

Tel. : / Fax :

The Mechanics of the Dental Anesthetic Cartridge

INTEGRAL-BONNET NEEDLE VALVES H-300 SERIES

Nondestructive Testing Procedure: Liquid Penetrant Testing

Draft for comments only Not to be cited as East African Standard

Kondomer av naturgummilatex Krav och provningsmetoder (ISO 4074:2002) Natural latex rubber condoms Requirements and test methods (ISO 4074:2002)

Packaging technology and preservation of foods Fátima Poças Biotechnology Faculty Universidade Católica Portuguesa 2017

Vasco Surgical Powder-free Sterile Surgical and Protective Gloves

--> Buy True-PDF --> Auto-delivered in 0~10 minutes. YY/T Translated English of Chinese Standard: YY/T

TRANSCRIPT for Lantus SoloSTAR pen injection for your patients

INSTRUCTIONS FOR PREPARING AND GIVING AN INJECTION OF ENBREL POWDER

Vasco Nitril long sterile Sterile Examination and Protective Gloves

Technical Specifications for the manufacture of: CANNED BEEF

Vasco Nitril Soft blue Non sterile Examination and Protective Gloves

Vasco Surgical Chloroprene Sterile Surgical and Protective Gloves

Part 1: General requirements

Instructions for Use. IJ Catheter Ultrasound Model Version 2400 Series

HumaPen LUXURA HD INSULIN DELIVERY DEVICE INSTRUCTIONS FOR USE

Tobacco Plain Packaging Regulations

Chapter 5: Checking and Maintaining Ultrasound Equipment

Vasco Nitril blue Non sterile Examination and Protective Gloves

Product: Spinal Needle. Zhejiang Runqiang Medical Instruments Co., Ltd

TRAINING PROGRAM CUPID FEMALE CONDOM

YY Translated English of Chinese Standard: YY

Qualification and Performance Specification for Rigid Printed Boards

Draft Indian Standard CINNAMON WHOLE SPECIFICATION (Second Revision of IS 4811)

PCR-C November 2003 W/CHANGE Jan 12 SECTION C

B. Braun Melsungen AG confirms that Vasco Guard long gloves comply with the following standards and directives: EN , ISO , ASTM D6319

For use only with Lilly 3 ml insulin cartridges (100 units/ml). Do not use other brands of insulin cartridges.

Draft Indian Standard WHEAT BRAN AS LIVESTOCK FEED SPECIFICATION (Second Revision of IS 2239)

ISO INTERNATIONAL STANDARD. Dentistry Reversible-irreversible hydrocolloid impression material systems

For use only with Lilly 3 ml insulin cartridges (100 units/ml). Do not use other brands of insulin cartridges.

Draft Indian Standard SPECIFICATION FOR DEHYDRATED ONION (First Revision)

TOOTH ISOLATION. the Rubber Dam. Dr. Ahmed Al-Jobory

PCR-R-015, ROTINI WITH CHEESE SAUCE, CHICKEN, TOMATOES AND ASPARAGUS, COOKED, DEHYDRATED, PACKAGED IN A BRICKPACK POUCH, SHELF STABLE

REVISION OF MONOGRAPH ON TABLETS. Tablets

USJ-875. Thank you for purchasing the USJ-875 SQUARE BIKE. Please read this manual carefully to ensure optimum performance and safety.

Dentistry Pre-capsulated dental amalgam

Data Pack. KIMTECH PURE* G3 Sterile Latex Gloves

QUALITY ASSURANCE. UNFPA Quality Assurance Framework for the Procurement of Reproductive Health Commodities

Elcometer 138/2. Surface Contamination Kit. Operating Instructions

DRIED NOODLES - Indonesia

IPC-6018A. Microwave End Product Board Inspection and Test IPC-6018A. A standard developed by IPC. Supersedes IPC-6018 January 1998

ISO INTERNATIONAL STANDARD. Sterile single-use intravascular catheter introducers

For use only with INSTRUCTIONS FOR USE

Vasco Nitril light Non sterile Examination and Protective Gloves

PCR-D-002B 13 August 2012 W/Change Sep 13 SUPERSEDING PCR-D-002A 28 September 2007 SECTION C

limbsandthings.com Advanced Catheterisation Trainer User Guide For more skills training products visit Limbs & Things Ltd.

13: Condoms. Words of Wisdom. How to Use a Male Condom. Condom Line-Up Cards. Shopping Information Form. Condoms Dos & Don ts

Toxicology Blood Lead Comprehensive Testing

Micronutrient powder - children 6-59 months - Cuba

Breakthrough Performance

DECISIONS. (Text with EEA relevance)

Version No.: 5.0 TITLE: SDS FOR FECAL OCCULT BLOOD TEST KIT T1-CK SERIES Page 1 of 5

I n s t r u c t i o n M a n u a l

Instructions for Use Enbrel (en-brel) (etanercept) for injection, for subcutaneous use Multiple-dose Vial

Instructions for Use Enbrel (en-brel) (etanercept) Single-use Prefilled SureClick Autoinjector

Technical Specifications for the manufacture of: FORTIFIED NIXTAMALIZED MAIZE FLOUR HONDURAS AND RBP Local 1 Regional

Advanced Catheterisation Trainer User Guide

Vasco OP Underglove Sterile Surgical and Protective Gloves

CENTRAL MARKS DEPARTMENT II (Legal) Our Ref: CMD-II(L)/16: February 2015

Protn-Latex. For Determination of Protein in Latex. (Cat. # Latex, Latex) think proteins! think G-Biosciences

EDICT ± OF GOVERNMENT

CLICK SEAL SYSTEM. Thermo Scientific Samco Clicktainer Vial. Unique click seal system providing sample protection and user safety

Experimental Procedure

How to Use ENBREL : Vial Adapter Method

STANDARD FOR QUICK FROZEN FISH FILLETS CODEX STAN Adopted in Revised in Amended in 2011, 2013, 2014.

Instructions for Use. Welcome!

SUPERBKLEAN! MAGNETIC SANITARY NAPKIN!

Non-destructive testing Penetrant testing. Part 2: Testing of penetrant materials

HumaPen SAVVIO INSULIN DELIVERY DEVICE INSTRUCTIONS FOR USE

Toxicology Blood Lead Comprehensive Testing

3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing Description 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing is used

A GUIDE TO OUR EXCLUSIVE FAMILY OF GLOVE PRODUCTS

AHDAA application for Halal Certification For the purpose of application to AHDAA for Halal certification

Products for a Fast and Reliable Fill

Non-Destructive Testing (NDT)

Preventing Sexually Transmitted Infections Storytelling Activity

Sterile hypodermic syringes for single use. Part 1: Syringes for manual use

Transcription:

ANNEX III: MALE CONDOM INSPECTION, SAMPLING AND TESTING SPECIFICATIONS Prior to shipment, each consignment of condoms will be sampled by an independent inspection company appointed by UNFPA at the factory or manufacturer s warehouse, in accordance with ISO 2859-1 1 and the technical specifications that govern the respective agreement. The costs associated with the first inspection of each batch shall be borne by UNFPA. In the case of rejection, the cost of subsequent inspection(s) shall be borne by the male condom manufacturer. These samples will then be tested by the independent testing laboratory, in accordance with the methods stated in ISO 4074 and the WHO/UNFPA Male Latex Condom Specification 2010 2. All testing activities will be conducted under ISO 17025 accreditation. Annex III is prepared in accordance with ISO 4074, the WHO/UNFPA Male Latex Condom Specification 2010 and UNFPA specific requirements for condoms. Should there be discrepancy between Annex III, ISO 4074, and WHO/UNFPA Male Latex Condom Specification 2010, the highest and strictest requirements of the three will prevail. A. Dimensions Inspection Level S-2. Length: Measurement of condom length will be taken in accordance with the relevant clauses and annexes of ISO 4074. WHO/UNFPA specifies that the condom s minimum length, unless otherwise specified in the UNFPA purchase order, will be: 165 mm for condoms less than 50.0 mm wide; 180 mm for condoms 50.0 to 55.5 mm wide; 190 mm for condoms equal to or wider than 56.0 mm. The compliance level for each lot will be an AQL of 1.0. Test report: The test report will include the elements of relevant clauses and annexes of ISO 4074 and the length of each tested condom. Width: Measurement of condom width will be taken in accordance with the relevant clauses and annexes of ISO 4074. Standard widths for public sector condoms are 49 mm or 53 mm. The required width will be specified in the UNFPA purchase order. A tolerance of ± 2 mm for individual condoms will apply. The compliance level for each lot will be an AQL of 1.0. 1 For undated standards, the most recent edition will apply 2 WHO/UNFPA Male Latex Condom: Specification, Prequalification and Guidelines for Procurement, 2010

Test report: The test report will include the elements of relevant clauses and annexes of ISO 4074 and the width of each tested condom, including the point, along the condom, at which the measurement was taken. Wall thickness: Measurement of condom wall thickness will be taken in accordance with the relevant clauses and annexes of ISO 4074. The wall thickness of condoms will be measured at three points: (30 ± 5) mm from the open end, (30 ± 5) mm from the closed end, and at the mid-distance between these two points. Lateral measurements made from the closed end will exclude the reservoir tip. The individual measurements and the average of all three measurements will be recorded for each condom. Measurements will be taken with a micrometer (dial or digital types are acceptable) with a resolution of at least 0.001mm, a flat foot contact of diameter between 3mm and 7mm, and a foot pressure of (22 ± 5) kpa. For convenience of measurement, double wall thickness may be measured and divided by two. Before measurement, condoms will be wiped once, inside and out, with absorbent tissue. WHO/UNFPA specifies that the condom s mean single-wall thickness (calculated from the three individual measurements) for each condom will be (0.065 + 0.015 0.020) mm, unless otherwise specified in the UNFPA purchase order. The compliance level for each lot will be an AQL of 1.0. Test report: The test report will include the elements of the relevant clauses and annexes of ISO 4074, as well as the average calculated thickness of each tested condom. Shape and texture: Determination of shape and texture will be made by visual inspection, in accordance with the WHO/UNFPA Male Latex Condom Specification 2010. The condom will be of natural color, parallel-sided, without constrictions and with a visible shoulder leading to a reservoir tip, unless otherwise specified in the UNFPA purchase order. B. Quantity of lubricant Inspection Level S-2. Measurement of lubricant amount in the condom package will be made in accordance with the relevant clauses and annexes of ISO 4074 and the WHO/UNFPA Male Latex Condom Specification 2010. The total quantity of lubricant in a package, including powder, will be (550 ± 150) mg. The compliance level will be an AQL of 4.0. Note: WHO/UNFPA specifies that silicone fluid with a viscosity between 200 and 350 centistokes shall be used as the lubricant and a dusting powder such as cornstarch, magnesium carbonate and/or calcium carbonate should be used to prevent the condoms sticking together during manufacture. The maximum recommended level of powder is 50mg per condom. C. Bursting volume and pressure test Sampling and inspection: Sampling and inspection are performed in accordance with ISO 2859-1, General Inspection Level G-1 for testing before and after oven conditioning.

Testing will be performed in accordance with the relevant clauses and annexes of ISO 4074. Note: For standard UNFPA orders, testing for bursting pressure and volume after oven conditioning is not required. In the exceptional cases where oven-treatment is required, this will be expressly stated in the UNFPA Purchase Order. The compliance level for each lot will be an AQL of 1.5 for non-conforming condoms. The minimum burst requirements for the condoms (both before and, if appropriate, after oven conditioning) will be as follows: Volume: Pressure: 16.0 dm 3 for condoms with widths less that 50.0 mm 18.0 dm 3 for condoms with widths from 50.0 mm up to but not including 56.0 mm 22.0 dm 3 for condoms with widths greater than or equal to 56.0 mm 1.0 kpa for all condoms Test report: The test report will include elements from the relevant clauses and annexes of ISO 4074 and the bursting volume and bursting pressure of each tested condom. D. Freedom-from-holes and visible defects Sampling and inspection: Sampling and inspection are performed in accordance with ISO 2859-1, General Inspection Level G-1, but at least Code Level M. Condoms will be tested in accordance with the relevant clauses and annexes of ISO 4074. The compliance level for freedom-from-holes (the sum of condoms with visible and non-visible holes and tears) will be an AQL of 0.25. The following will be considered non-compliers for holes: Condoms which burst during tests Condoms which break during mounting on the test head Condoms which show any evidence of leakage, including seepage, micro-droplets, and squirters. However, leakage within a distance of 25mm (1 inch) or less from the rim (open end) may be disregarded. Condoms which have visible holes or tears before the water is added (including visible holes or tears less than 25mm from the rim). The compliance level for critical visible defects is 0.4. The compliance level for non-critical visible defects is 2.5. Visible defects are defined as follows: Critical visible defects (AQL 0.4)

Defect Description Pleat/crease The film sticks to itself, and the pleat/crease cannot be removed by gentle stretching of the adjacent film. Blister/bubble An obvious circular or teardrop-shaped thin area with a well-defined border in the film (such defects may break under pressure). Coagulum (large) Rubber particles with any dimension greater than 1mm. These may cause the condom to fail in use. Embedded and Any particle with a dimension of 1mm or greater. These may be dirt, hair, insects etc.. surface particles Bead defects Faulty, missing or severely distorted beads (as in ISO 4074). Crack marks Lines that penetrate the surface of the film, formed by shrinkage of the latex during drying. These do not include flow lines or marks from the mould. Delamination Areas where the individual layers of latex separate (condoms are formed by two or more dips in the liquid latex). Thin areas Small areas of the condom (including the teat) that are visibly thin. These can show up as bulges with well-defined edges on the freedom-from-holes test. Condoms that look asymmetrical when filled with water are not necessarily in this category. Non-critical visible defects (AQL 2.5) Defect Embedded and surface particles (small) Faulty bead (minor) Uneven color Description Particles with dimensions less than 1mm that are visible to the naked or corrected eye. Uneven and partially distorted beads. Minor streaking. Occasionally, imperfections can be seen in condoms that do not affect the performance or acceptability of the product. No action should be taken when these imperfections are seen. Common imperfections are: Imperfections that are not regarded as defects Phenomenon Description Micro-coagulum Particles of rubber with dimensions less than 1mm. Flow lines Lines of denser material in the film. Concave spot at An apparent indentation caused during withdrawal of the former (dipping end of teat mould) from the latex. Distortion due to Apparent variations in condom width due to stretching during rolling. rolling Bulges Large bulges or distortion of the condom during the freedom-from-holes test that are due to differences in thickness around the wall of the condom caused by relative movement of the latex and the former (dipping mould) during dipping (these may or may not have well-defined edges). Uneven lubricant The open end of the condom may appear dry, especially on new condoms. The lubricant penetrates the roll slowly. Test report: The test report will include elements from the relevant clauses and annexes of ISO 4074 and the following particulars: The number of condoms exhibiting a visible hole or tear before mounting on the apparatus;

The number of condoms exhibiting a voltage equal to or greater than 50mV (in the case of electrical tests); The number of condoms with leaks observable on the apparatus which, when measured, are located more than 25mm from the open end; The number of condoms which show signs of leakage on rolling, which, when measured, are located more than 25mm from the open end; The number of condoms with visible defects other than holes or tears, and the nature of the defects. E. Package integrity: Inspection Level S-3 Testing will be performed in accordance with the relevant clauses and annexes of ISO 4074, to check for possibility of breaches in sealed individual condom containers that may result in leakage of lubricant. The compliance level for each lot will be an AQL of 2.5. F. Individual package materials and markings: Inspection Level S-3. The sample of condom packages will be visually inspected to verify the required aspects of package quality. Quantitative tests to measure these parameters are not required, except for measurement of the thickness of the aluminum foil package. The compliance level for each lot will be an AQL of 2.5. The sample of condom packages is inspected with the following requirements: The color, print design and identification marking, including Pantone references and font sizes, will be as specified by the UNFPA purchase order; Individual packages will be square or circular as specified in the UNFPA purchase order and will not distort the rolled condom. They will be hermetically sealed and shall protect the product form oxygen, ozone water vapor, and ultraviolet and visible light; Unless otherwise stated in the UNFPA purchase order, the package will be constructed from a laminate which includes a layer of suitable impermeable flexible aluminum foil. The layer of each aluminum foil will have a minimum thickness of 8 micrometers. The layers of plastic materials will be suitable for mechanical protection of the metal foil and for printing and sealing. The thickness of the aluminum foil (including laminate) will be verified by a micrometer. However, UNFPA looks

forward to the testing laboratory s expertise on measurement of foil only or foil with laminate, depending upon the available technology; Any lot numbers and expiration dates will be printed on packages at the time of packaging, not pre-printed. In addition, the following will apply: There will be no evidence of leakage; The outside surface of the package will be clean and free from lubricant; There will be no separation of the layers of the laminate; If the sealed packages are in strips, the individual packages will be separated by perforations which allow the packages to be separated by hand without interfering with the seals; The packages will be easy to open without damaging the condom; In addition, the visual inspection will verify that the identification marking on the packages is complete and correct, as specified by the UNFPA buyer or the UNFPA purchase order. WHO requires the following particulars to be shown on the condom packages: Manufacturer s name; Batch or lot identification code (printed at the time of packaging, not pre- printed); Month and year of expiry labeled Expiry Date in a language to be specified by the buyer (Month/Year, xx/xxxx); Month and year of manufacturing date, if specified in the UNFPA purchase order; Other information specified in UNFPA s purchase order. Test report: The test report will include the elements of the relevant clauses and annexes of ISO 4074, as well as the following particulars: The number of containers with detected leaks from air-bubbles; The number of containers with detected leaks of fluid inside the container. G. Test report The condom testing report will be prepared in accordance with the relevant clauses and annexes of ISO 4074. H. Inspection of Packing and Marking An inspection shall be performed to ensure that packaging, packing, and marking are in compliance with the requirements of WHO Model Specifications Section 3.4. The inspection shall be conducted in accordance with ISO 2859-1. For inspection related to the exterior shipping cartons, the sample unit shall be one exterior shipping carton. For inspections related to other parameters, the lot size shall be the number of inner boxes and the sample unit shall be one inner box. The inspection level shall be S-3, with an AQL of 2.5. Examination of inner boxes shall be performed on packages selected at random from sample shipping cartons. Examination of defects of closure shall be performed on randomly selected shipping cartons fully prepared for delivery. Preparation for delivery defects shall be scored in accordance with the Table below: Classification for Defects in Packaging and Marking:

Examine Content Markings Materials Workmanship Defects Number of condoms not as specified; packets or strips not as specified Omitted, incorrect, illegible, or of improper size, location, sequence, or method of application Packaging/packing materials not as specified, missing, damaged or non serviceable Shipping cartons inadequately closed or secured; poor application of internal packaging and packing material; distorted intermediate packages