Identity
- Trade Name
- Search-Cyte Pool 0.8% FDA UDI
- Generic Name
- Pooled antibody screening reagent red blood cell IVD, antigen FDA UDI
- Device Name
- Reagent Red Blood Cells for use in the detection of unexpected antibodies in gel technique. For in vitro diagnostic use FDA UDI
- Model / Reference
- 3x10 ml FDA UDI
- Description
- Reagent Red Blood Cells for use in the detection of unexpected antibodies in gel technique. For in vitro diagnostic use FDA UDI
Identifiers
- Catalog Number
- 213289 FDA UDI
- Primary DI / UDI-DI
- 07640137341596 FDA UDI
- GMDN Term
- Pooled antibody screening reagent red blood cell IVD, antigen FDA UDI
Classification
- 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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: Pooled antibody screening reagent red blood cell IVD, antigen
Search-Cyte Pool 0.8% by Medion Grifols Diagnostics AG — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pooled antibody screening reagent red blood cell IVD, antigen.
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
- Medion Grifols Diagnostics AG
Sources (1)
- FDA UDI 8c2c0a7f-924e-4ebd-9107-92e583b1cb04 33 fields · synced May 30, 2026