Identity
- Trade Name
- KOVA FDA UDI
- Generic Name
- Centrifuge tube IVD FDA UDI
- Device Name
- KO-LEC-PAC, 500 Determinations FDA UDI
- Model / Reference
- 87141 FDA UDI
- Description
- KO-LEC-PAC, 500 Determinations FDA UDI
Identifiers
- Catalog Number
- 87141 FDA UDI
- Primary DI / UDI-DI
- 00855617006934 FDA UDI
- FDA Product Code
- NNK FDA UDI
- GMDN Term
- Centrifuge tube IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3250 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
No
FDA UDI
Category: General specimen microscopy slide IVD, single-useCentrifuge tube IVDUser-induced pipette
Kova by Kova International Inc — 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
- Kova International Inc
Sources (1)
- FDA UDI 9c885c8f-1522-4462-9a52-0c509cc9258c 36 fields · synced May 29, 2026