Identity
- Trade Name
- Progen PRP Eclipse FDA UDI
- Generic Name
- Blood collection set, invasive FDA UDI
- Device Name
- 30 ml Blood Draw Kits FDA UDI
- Model / Reference
- TN30MLSINGLE FDA UDI
- Description
- 30 ml Blood Draw Kits FDA UDI
Identifiers
- Catalog Number
- F5PG014.02 FDA UDI
- Primary DI / UDI-DI
- 00850035498385 FDA UDI
- FDA Product Code
- PQD FDA UDI
- GMDN Term
- Blood collection set, invasive FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1675 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Blood collection set, invasive
Progen PRP Eclipse by Bellus Medical, Llc — 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
- Bellus Medical, Llc
Sources (1)
- FDA UDI 520127a7-f5e1-46e6-833b-a78e63018503 35 fields · synced May 30, 2026