Identity
- Trade Name
- Human Fetal Hemoglobin Test Kit FDA UDI
- Generic Name
- Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Model / Reference
- HFH04 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10190302005340 FDA UDI
- 510(k) Number
- K990641 FDA UDI
- FDA Product Code
- GHQ FDA UDI
- GMDN Term
- Multiple solid tumour differentiation marker IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.7455 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
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
Human Fetal Hemoglobin Test Kit by Life Technologies Limited — 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
- Life Technologies Limited
Sources (1)
- FDA UDI a37e1d0a-6052-4a9a-b6a5-ad2fc542f191 34 fields · synced Jun 8, 2026