NF EN ISO 9187-1

NF EN ISO 9187-1

May 2008
Standard Cancelled

Injection equipment for medical use - Part 1 : ampoules for injectables

ISO 9187-1:2006 specifies materials, dimensions, capacities, performance and packaging requirements for three forms of glass ampoule (forms B, C and D) for injectable pharmaceutical products.It is applicable to ampoules with and without a colour break-ring.The provision of ampoules with a colour break-ring, and the choice of colour of the break-ring, is subject to agreement between the manufacturer and user.Ampoules complying with ISO 9187-1:2006 are intended for single use only.

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Main informations

Collections

National standards and national normative documents

Publication date

May 2008

Number of pages

14 p.

Reference

NF EN ISO 9187-1

ICS Codes

11.040.20   Transfusion, infusion and injection equipment

Classification index

S93-130-1

Print number

1 - 29/04/2008

International kinship

ISO 9187-1:2006

European kinship

EN ISO 9187-1:2008
Sumary
Injection equipment for medical use - Part 1 : ampoules for injectables

ISO 9187-1:2006 specifies materials, dimensions, capacities, performance and packaging requirements for three forms of glass ampoule (forms B, C and D) for injectable pharmaceutical products.

It is applicable to ampoules with and without a colour break-ring.

The provision of ampoules with a colour break-ring, and the choice of colour of the break-ring, is subject to agreement between the manufacturer and user.

Ampoules complying with ISO 9187-1:2006 are intended for single use only.

Replaced standards (1)
NF EN ISO 9187-1
August 2003
Standard Cancelled
Injection equipment for medical use - Part 1 : ampoules for injectables

Le présent document spécifie les matériaux, les dimensions, les capacités et les exigences de performance et d'emballage des trois types d'ampoules en verre (types B, C et D) pour produits injectables. Il s'applique aux ampoules avec ou sans anneau de cassure coloré.

Standard replaced by (1)
NF EN ISO 9187-1
December 2010
Standard Current
Injection equipment for medical use - Part 1 : ampoules for injectables

ISO 9187-1:2010 specifies materials, dimensions, capacities, performance and packaging requirements for three forms of glass ampoule (forms B, C and D) for injectable pharmaceutical products. ISO 9187-1:2010 is applicable to ampoules with and without a colour break-ring; the provision of ampoules with a colour break-ring, and the choice of colour of the break-ring, is subject to agreement between the manufacturer and user. Ampoules complying with ISO 9187-1:2010 are intended for single use only.

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