Identity
- Trade Name
- Referencells A2 FDA UDI
- Generic Name
- Group A2 Rh (D) positive reagent red blood cell IVD, antigen FDA UDI
- Device Name
- This configuration of the product contains one (1) vial, namely known A2 red blood cells, and is used for the confirmation of reverse expected ABO serum grouping antibodies. FDA UDI
- Model / Reference
- 0002342 FDA UDI
- Description
- This configuration of the product contains one (1) vial, namely known A2 red blood cells, and is used for the confirmation of reverse expected ABO serum grouping antibodies. FDA UDI
Identifiers
- Catalog Number
- 0002342 FDA UDI
- Primary DI / UDI-DI
- 10888234000266 FDA UDI
- GMDN Term
- Group A2 Rh (D) positive reagent red blood cell IVD, antigen 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: Group A2 Rh (D) positive reagent red blood cell IVD, antigen
Referencells A2 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 d155fd7b-c5d1-4a9c-b8b0-9151a5d82920 35 fields · synced May 29, 2026