Identity
- Trade Name
- MP Biomedicals LLC FDA UDI
- Generic Name
- Gastrin IVD, kit, radioimmunoassay FDA UDI
- Device Name
- GASTRIN RIA 125I 200 TUBE KIT FDA UDI
- Model / Reference
- 06B255025 FDA UDI
- Description
- GASTRIN RIA 125I 200 TUBE KIT FDA UDI
Identifiers
- Catalog Number
- 06B255025 FDA UDI
- Primary DI / UDI-DI
- 00817830023136 FDA UDI
- FDA Product Code
- CGC FDA UDI
- GMDN Term
- Gastrin IVD, kit, radioimmunoassay FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1325 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Gastrin IVD, kit, radioimmunoassay
MP Biomedicals LLC by Mp Biomedicals, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Gastrin IVD, kit, radioimmunoassay.
- Gastrin - RIA — Diasource Immunoassays, S.A. · Class I
- EURIA Gastrin — Euro-Diagnostica AB · Class I
- MP Biomedicals LLC — MP BIOMEDICALS, LLC · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Mp Biomedicals, Llc
Sources (1)
- FDA UDI d9b4550b-25c0-4f2a-a2de-22a6c32fbff0 34 fields · synced Jun 1, 2026