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BS EN ISO 7886-2:2020 Sterile hypodermic syringes for single use - Syringes for use with power-driven syringe pumps >
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BS EN ISO 7886-2:2020 Sterile hypodermic syringes for single use - Syringes for use with power-driven syringe pumps, 2024
- undefined
- Foreword
- Introduction
- 1 Scope
- 2 Normative references
- 3 Terms and definitions
- 4 Nomenclature
- 5 General requirements
- 6 Limits for acidity or alkalinity
- 7 Limits for extractable metals
- 8 Lubricant
- 9 Tolerance on graduated capacity
- 10 Graduated scale
- 11 Syringe design
- 12 Piston/plunger assembly
- 12.1 Design
- 12.2 Fit of plunger stopper/plunger in barrel
- 13 Nozzle
- 13.1 Conical fitting
- 13.2 Nozzle lumen
- 14 Performance
- 14.1 Dead space
- 14.2 Freedom from air and liquid leakage past the plunger stopper
- 14.3 Short-term flow rate error
- 14.4 Pump forces
- 14.5 Syringe compliance
- 15 Packaging
- 15.1 Unit packaging and self-contained syringe units
- 15.1.1 Unit packaging
- 15.1.2 Self-contained syringe units
- 15.2 Multiple unit pack
- 15.3 User packaging
- 16 Information supplied by the manufacturer
- 16.1 General
- 16.2 Syringes
- 16.2.1 General
- 16.2.2 Additional marking for self-contained syringe units
- 16.3 Unit packaging
- 16.4 Multiple unit packs
- 16.4.1 General
- 16.4.2 Multiple unit packs with self-contained syringes
- 16.5 User packaging
- 16.6 Storage container
- 16.7 Transport wrapping
- Annex A (normative) Short-term flow rate accuracy
- Annex B (informative) Pump force
- Annex C (normative) Determination of syringe compliance
- Bibliography [Go to Page]
