Identity
- Trade Name
- MINICAP CDT MAXI KIT FDA UDI
- Generic Name
- Transferrin/transferrin isoform IVD, kit, electrophoresis FDA UDI
- Device Name
- CARBOHYDRATE DEF TRANSFERRIN BY CE MINICAP FDA UDI
- Model / Reference
- 2228 FDA UDI
- Description
- CARBOHYDRATE DEF TRANSFERRIN BY CE MINICAP FDA UDI
Identifiers
- Catalog Number
- 2228 FDA UDI
- Primary DI / UDI-DI
- 03607360022283 FDA UDI
- FDA Product Code
- NAO FDA UDI
- GMDN Term
- Transferrin/transferrin isoform IVD, kit, electrophoresis FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1360 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
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: Transferrin/transferrin isoform IVD, kit, electrophoresis
Minicap Cdt Maxi Kit by Sebia, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Sebia, Inc.
Sources (1)
- FDA UDI 18222134-5eeb-4e0e-9957-bbc66f233df9 35 fields · synced May 31, 2026