Identity
- Trade Name
- PermaLife FDA UDI
- Generic Name
- Blood/tissue storage/culture container FDA UDI
- Device Name
- PermaLife Cell Culture Bag, 500ml, "P" Set, packed with additional PVC spike port FDA UDI
- Model / Reference
- PL500P FDA UDI
- Description
- PermaLife Cell Culture Bag, 500ml, "P" Set, packed with additional PVC spike port FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10816203021844 FDA UDI
- FDA Product Code
- LPZ FDA UDI
- GMDN Term
- Blood/tissue storage/culture container FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not 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
PermaLife by OriGen Biomedical, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 U | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- OriGen Biomedical, Inc.
Sources (1)
- FDA UDI 886eb41c-8fb0-41de-9479-fe43ae95f0a2 35 fields · synced Jun 1, 2026