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Factor V Deficient Substrate Plasma

FDA UDI

Class II (US FDA UDI)

by Helena Laboratories, Corp.

Identity

Trade Name
Factor V Deficient Substrate Plasma FDA UDI
Generic Name
Coagulation factor V IVD, reagent FDA UDI
Model / Reference
5191 FDA UDI

Identifiers

Primary DI / UDI-DI
M52551910 FDA UDI
510(k) Number
K792507 FDA UDI
FDA Product Code
GGP FDA UDI
GMDN Term
Coagulation factor V 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

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: Coagulation factor V IVD, reagent

Factor V Deficient Substrate Plasma by Helena Laboratories, Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coagulation factor V IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db18dac1-2d24-42e1-b49b-f6f5eb63ec2d 34 fields · synced Jun 9, 2026