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STA® - Staclot® Protein C 3

FDA UDI

Class II (US FDA UDI)

by Diagnostica Stago, Inc.

Identity

Trade Name
STA® - Staclot® Protein C 3 FDA UDI
Generic Name
Protein C IVD, kit, clotting FDA UDI
Model / Reference
00737 FDA UDI

Identifiers

Primary DI / UDI-DI
03607450007374 FDA UDI
510(k) Number
K861079 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Protein C IVD, kit, clotting

STA® - Staclot® Protein C 3 by Diagnostica Stago, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Protein C IVD, kit, clotting.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cab53647-ec06-4940-b688-afbfc190b75b 34 fields · synced May 30, 2026