Identity
- Trade Name
- Primrose Medical, Inc FDA UDI
- Generic Name
- Subcutaneous infusion/injection port needle FDA UDI
- Device Name
- Sub-Q ( subcutaneous ) Administration set, Safety FDA UDI
- Model / Reference
- 900-5111 FDA UDI
- Description
- Sub-Q ( subcutaneous ) Administration set, Safety FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00852323007255 FDA UDI
- FDA Product Code
- FPA FDA UDI
- GMDN Term
- Subcutaneous infusion/injection port needle FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 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
No
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
Category: Electric infusion pump administration set, single-useMechanical infusion pump administration setSubcutaneous infusion/injection port needleElectronic gravity infusion controller administration set
Primrose Medical, Inc by Primrose Medical, Inc. — 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
- Primrose Medical, Inc.
Sources (1)
- FDA UDI 71a40a1e-bb06-4ae2-9b03-f51c667979ab 33 fields · synced Jun 8, 2026