Identity
- Trade Name
- Lymphotype HLA-ABC 72 FDA UDI
- Generic Name
- HLA class I antigen tissue typing IVD, kit, complement-dependent cytotoxicity (CDC) FDA UDI
- Device Name
- for 6 detections of human HLA-ABC antigens in the complement-dependent microlymphocytotoxicity test FDA UDI
- Model / Reference
- 823020 FDA UDI
- Description
- for 6 detections of human HLA-ABC antigens in the complement-dependent microlymphocytotoxicity test FDA UDI
Identifiers
- Catalog Number
- 823020 FDA UDI
- Primary DI / UDI-DI
- 07611969952717 FDA UDI
- FDA Product Code
- MZI FDA UDI
- GMDN Term
- HLA class I antigen tissue typing IVD, kit, complement-dependent cytotoxicity (CDC) FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
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
Lymphotype HLA-ABC 72 by Bio-Rad Medical Diagnostics GmbH — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- Bio-Rad Medical Diagnostics GmbH
Sources (1)
- FDA UDI 5a491ec2-b3ee-4f8b-8466-6a917c7b43d8 37 fields · synced May 30, 2026