← Back to catalogue

Tina-quant CReactive Protein IV

FDA UDI

Class II (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Tina-quant CReactive Protein IV FDA UDI
Generic Name
C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI
Model / Reference
07876424190 FDA UDI

Identifiers

Catalog Number
07876424190 FDA UDI
Primary DI / UDI-DI
04015630946846 FDA UDI
510(k) Number
K192072 FDA UDI
FDA Product Code
DCN FDA UDI
GMDN Term
C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.5270 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: C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry

Tina-quant CReactive Protein IV by Roche Diagnostics Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as C-reactive protein (CRP) IVD, kit, nephelometry/turbidimetry.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c8915994-9b8f-42e8-a7b6-4bd94b158aaf 35 fields · synced Jun 1, 2026