Identity
- Trade Name
- Hemo-QC FDA UDI
- Generic Name
- Multiple blood group genotyping IVD, control FDA UDI
- Device Name
- Hemo-QC simulates blood samples and is intended for the daily quality control of routine blood bank reagents used in manual, semi-automated and automated blood typing and antibody screen test systems. FDA UDI
- Model / Reference
- H9200 FDA UDI
- Description
- Hemo-QC simulates blood samples and is intended for the daily quality control of routine blood bank reagents used in manual, semi-automated and automated blood typing and antibody screen test systems. FDA UDI
Identifiers
- Catalog Number
- H9200 FDA UDI
- Primary DI / UDI-DI
- 00858352006009 FDA UDI
- FDA Product Code
- KSF FDA UDI
- GMDN Term
- Multiple blood group genotyping IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9650 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Multiple blood group genotyping IVD, control
Hemo-QC by Hemo Bioscience — 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
- Hemo Bioscience
Sources (1)
- FDA UDI 72b83b54-52d3-4141-a154-14c48d92c92d 36 fields · synced May 30, 2026