Identity
- Trade Name
- Tina-quant Cystatin C Gen.2 FDA UDI
- Generic Name
- Cystatin C IVD, kit, nephelometry/turbidimetry FDA UDI
- Model / Reference
- 08105596190 FDA UDI
Identifiers
- Catalog Number
- 08105596190 FDA UDI
- Primary DI / UDI-DI
- 07613336133644 FDA UDI
- 510(k) Number
- K161817 FDA UDI
- FDA Product Code
- NDY FDA UDI
- GMDN Term
- Cystatin C IVD, kit, nephelometry/turbidimetry FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1225 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
Yes
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: Cystatin C IVD, kit, nephelometry/turbidimetry
Tina-quant Cystatin C Gen.2 by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Cystatin C IVD, kit, nephelometry/turbidimetry.
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- Diazyme — Diazyme Laboratories, Inc.
- N Latex Cystatin C — SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD · Class II
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- Optilite Cystatin C Kit — The Binding Site Group · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Roche Diagnostics Corp.
Sources (1)
- FDA UDI cb0f9ddf-f002-4680-8a07-98606492459b 35 fields · synced Jun 6, 2026