Identity
- Trade Name
- Follett FDA UDI
- Generic Name
- Blood plasma freezer FDA UDI
- Device Name
- Freezer, upright, 20 cu.ft, Right hinge, chart recorder and heated door FDA UDI
- Model / Reference
- FZR20-PL-RHTCR FDA UDI
- Description
- Freezer, upright, 20 cu.ft, Right hinge, chart recorder and heated door FDA UDI
Identifiers
- Catalog Number
- 00979203 FDA UDI
- Primary DI / UDI-DI
- 00857117006230 FDA UDI
- FDA Product Code
- KSE FDA UDI
- GMDN Term
- Blood plasma freezer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9700 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Follett by Follett Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Follett Corporation
Sources (1)
- FDA UDI ade709ad-6a89-460f-8d12-a09c69d6a3e9 35 fields · synced Jun 6, 2026