Identity
- Trade Name
- Anti-Dia FDA UDI
- Generic Name
- Anti-Di^a red blood cell grouping IVD, antibody FDA UDI
- Device Name
- This reagent is used for the detection of the Di(a) antigen on red blood cells by tube test. This product configuration is a single vial. FDA UDI
- Model / Reference
- 0007620 FDA UDI
- Description
- This reagent is used for the detection of the Di(a) antigen on red blood cells by tube test. This product configuration is a single vial. FDA UDI
Identifiers
- Catalog Number
- 0007620 FDA UDI
- Primary DI / UDI-DI
- 10888234000839 FDA UDI
- GMDN Term
- Anti-Di^a red blood cell grouping IVD, antibody FDA UDI
Classification
- Commercial Distribution
- 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
No
FDA UDI
Combination Product
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: Anti-Di^a red blood cell grouping IVD, antibody
Anti-Dia by Immucor, Inc. — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Immucor, Inc.
Sources (1)
- FDA UDI c5d2fd3c-a6f6-48ba-86d0-3ffd9050ec71 35 fields · synced May 30, 2026