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Protein C Reagent

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics Products Ltd

Identity

Trade Name
Protein C Reagent FDA UDI
Generic Name
Protein C IVD, kit, clotting FDA UDI
Device Name
Coagulation test for the quantitative determination of protein C activity in human plasma FDA UDI
Model / Reference
10446185 FDA UDI
Description
Coagulation test for the quantitative determination of protein C activity in human plasma FDA UDI

Identifiers

Catalog Number
OQYG11 FDA UDI
Primary DI / UDI-DI
00842768008641 FDA UDI
510(k) Number
K002541 FDA UDI
FDA Product Code
GGP FDA UDI
GMDN Term
Protein C IVD, kit, clotting FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7290 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

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: Protein C IVD, kit, clotting

Protein C Reagent by Siemens Healthcare Diagnostics Products Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Protein C IVD, kit, clotting.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1d83cd57-bb7e-4c05-838c-3747fb898353 37 fields · synced May 30, 2026