Identity
- Trade Name
- Xpert Check FDA UDI
- Generic Name
- Thermal cycler nucleic acid instrument calibrator/control kit IVD FDA UDI
- Device Name
- Xpert Check; 5 each per kit FDA UDI
- Model / Reference
- XPERTCHECK-US-5 FDA UDI
- Description
- Xpert Check; 5 each per kit FDA UDI
Identifiers
- Catalog Number
- XPERTCHECK-US-5 FDA UDI
- Primary DI / UDI-DI
- 07332940001872 FDA UDI
- FDA Product Code
- OHQ FDA UDI
- GMDN Term
- Thermal cycler nucleic acid instrument calibrator/control kit IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1660 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
Yes
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
No
FDA UDI
Category: Thermal cycler nucleic acid instrument calibrator/control kit IVD
Xpert Check by Cepheid — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Cepheid
Sources (1)
- FDA UDI d2c4c911-e831-4c4b-8614-720742e20987 36 fields · synced Jun 8, 2026