Identity
- Trade Name
- BD PosiFlush FDA UDI
- Generic Name
- Vascular catheter/cannula flush solution, anticoagulant, non-antimicrobial FDA UDI
- Device Name
- SYRINGE 5ML HEPARIN 100 UNIT FDA UDI
- Model / Reference
- 306424 FDA UDI
- Description
- SYRINGE 5ML HEPARIN 100 UNIT FDA UDI
Identifiers
- Catalog Number
- 306424 FDA UDI
- Primary DI / UDI-DI
- 00382903064243 FDA UDI
- FDA Product Code
- NZW FDA UDI
- GMDN Term
- Vascular catheter/cannula flush solution, anticoagulant, non-antimicrobial FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5200 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 5 Milliliter FDA UDI
Category: Vascular catheter/cannula flush solution, anticoagulant, non-antimicrobial
BD PosiFlush by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI 9e3a0f0e-eded-4313-a801-044b4180c65f 36 fields · synced Jun 8, 2026