NS EN ISO 7886-3 : 2009
Current
The latest, up-to-date edition.
STERILE HYPODERMIC SYRINGES FOR SINGLE USE - PART 3: AUTO-DISABLE SYRINGES FOR FIXED-DOSE IMMUNIZATION
12-01-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Nomenclature
5 Cleanliness
6 Limits for acidity or alkalinity
7 Limits for extractable metals
8 Lubricant
9 Tolerance on nominal capacity
10 Graduated scale
11 Barrel
12 Piston/plunger assembly
13 Needle
14 Performance
15 Packaging
16 Labelling
Annex A (normative) Method for preparation of extracts
Annex B (informative) Test method for forces required to
operate plunger
Annex C (normative) Test method for testing auto-disable
feature
Annex ZA (informative) Relationship between this European
Standard and the Essential
Requirements of EU Directive
93/42 EEC
Bibliography
Specifies the properties and performance of sterile single-use hypodermic syringes with or without needle, made of plastic materials and stainless steel and intended for the aspiration of vaccines or for the injection of vaccines immediately after filling.
| DocumentType |
Standard
|
| PublisherName |
Norwegian Standards (Norges Standardiseringsforbund)
|
| Status |
Current
|
| SupersededBy |
| Standards | Relationship |
| DIN EN ISO 7886-3:2010-01 | Identical |
| NF EN ISO 7886-3 : 2009 | Identical |
| ISO 7886-3:2005 | Identical |
| NBN EN ISO 7886-3 : 2009 | Identical |
| NEN EN ISO 7886-3 : 2009 | Identical |
| I.S. EN ISO 7886-3:2009 | Identical |
| SN EN ISO 7886-3 : 2010 | Identical |
| UNI EN ISO 7886-3 : 2009 | Identical |
| BS EN ISO 7886-3:2009 | Identical |
| UNE-EN ISO 7886-3:2010 | Identical |
| EN ISO 7886-3:2009 | Identical |
| ONORM EN ISO 7886-3 : 2010 | Identical |
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