Identity
- Trade Name
- SAHARA FDA UDI
- Generic Name
- Multi-purpose warming cabinet, stationary FDA UDI
- Device Name
- Thawing device for stem cell preparations FDA UDI
- Model / Reference
- SAHARA-TSC 115V FDA UDI
- Description
- Thawing device for stem cell preparations FDA UDI
Identifiers
- Catalog Number
- 97.8710.602 FDA UDI
- Primary DI / UDI-DI
- 04028339720235 FDA UDI
- FDA Product Code
- KZL FDA UDI
- GMDN Term
- Multi-purpose warming cabinet, stationary FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9205 FDA UDI
- Commercial Distribution
- 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multi-purpose warming cabinet, stationary
Sahara by Transmed Medizintechnik GmbH & Co. KG — 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
- Transmed Medizintechnik GmbH & Co. KG
Sources (1)
- FDA UDI 52e6e31f-bb27-43db-b2be-8681b42ab8a5 34 fields · synced Jun 1, 2026