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Clostridium Difficile Glutamate Dehydrogenase(GDH) and Toxin A/B Detection Kit (
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Clostridium Difficile Glutamate Dehydrogenase(GDH) and Toxin A/B Detection Kit ( FDA UDI
- Generic Name
- Clostridium difficile antigen IVD, kit, rapid ICT, clinical FDA UDI
- Model / Reference
- 20 tests/kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06974849369236 FDA UDI
- FDA Product Code
- LLH FDA UDI
- GMDN Term
- Clostridium difficile antigen IVD, kit, rapid ICT, 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
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: Clostridium difficile antigen IVD, kit, rapid ICT, clinical
Clostridium Difficile Glutamate Dehydrogenase(GDH) and Toxin A/B Detection Kit ( by Jiangsu Macro & Micro-Test Med-Tech Co., Ltd. — Class I — FDA UDI — listed…
Similar devices
Also classified as Clostridium difficile antigen IVD, kit, rapid ICT, clinical.
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
- Jiangsu Macro & Micro-Test Med-Tech Co., Ltd.
Sources (1)
- FDA UDI 23ab448e-7e53-4083-88d4-e5fbc7a906bb 32 fields · synced May 31, 2026