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George King Factor VII Deficient Plasma

FDA UDI

Class II (US FDA UDI)

by George King Bio-Medical, Inc.

Identity

Trade Name
George King Factor VII Deficient Plasma FDA UDI
Generic Name
Coagulation factor VII IVD, reagent FDA UDI
Device Name
George King Factor VII Deficient Plasma is fresh frozen citrated human plasma derived from congenital Factor VII Deficient donors FDA UDI
Model / Reference
0700-1.0 FDA UDI
Description
George King Factor VII Deficient Plasma is fresh frozen citrated human plasma derived from congenital Factor VII Deficient donors FDA UDI

Identifiers

Primary DI / UDI-DI
00815696020054 FDA UDI
FDA Product Code
GJT FDA UDI
GMDN Term
Coagulation factor VII IVD, reagent 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

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: Coagulation factor VII IVD, reagent

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

Similar devices

Also classified as Coagulation factor VII IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ba9a9385-9765-43cb-8202-4e06db70b29c 35 fields · synced Jun 6, 2026