← Back to catalogue

George King Heparin Control Plasma

FDA UDI

Class II (US FDA UDI)

by George King Bio-Medical, Inc.

Identity

Trade Name
George King Heparin Control Plasma FDA UDI
Generic Name
Heparin anti-Xa IVD, control FDA UDI
Device Name
George King (GK) Heparin Control Plasma is an assayed citrated plasma intended for the control of Unfractionated Heparin (UFH) activity using an anti-Xa chromogenic assay and coagulation analyzer with appropriate commercial anti-Xa reagents. FDA UDI
Model / Reference
7000-1.0 FDA UDI
Description
George King (GK) Heparin Control Plasma is an assayed citrated plasma intended for the control of Unfractionated Heparin (UFH) activity using an anti-Xa chromogenic assay and coagulation analyzer with appropriate commercial anti-Xa reagents. FDA UDI

Identifiers

Primary DI / UDI-DI
00815696021327 FDA UDI
FDA Product Code
GGN FDA UDI
GMDN Term
Heparin anti-Xa IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.5425 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

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: Heparin anti-Xa IVD, control

George King Heparin Control Plasma by George King Bio-Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Heparin anti-Xa IVD, control.

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 991b1f90-e435-4aa7-b416-f04ab5e89c32 35 fields · synced May 30, 2026