Identity
- Trade Name
- PET RPLA KIT FDA UDI
- Generic Name
- Clostridium perfringens enterotoxin antigen IVD, kit, rapid agglutination, clinical FDA UDI
- Model / Reference
- TD0930A FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05032384028528 FDA UDI
- FDA Product Code
- JSP FDA UDI
- GMDN Term
- Clostridium perfringens enterotoxin antigen IVD, kit, rapid agglutination, clinical FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 866.2660 FDA UDI
- 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
No
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
Category: Clostridium perfringens enterotoxin antigen IVD, kit, rapid agglutination, clinical
Pet Rpla Kit by Oxoid Limited — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Oxoid Limited
Sources (1)
- FDA UDI 4b352e6a-8eb1-4e02-9d35-fc04cf8430b8 32 fields · synced May 30, 2026