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QuikClot

FDA UDI

Class U (US FDA UDI)

by Z-Medica, LLC

Identity

Trade Name
QuikClot FDA UDI
Generic Name
Non-organic haemostatic agent FDA UDI
Device Name
QuikClot Bleeding Control Kit, Stanford, OTC, CAT FDA UDI
Model / Reference
0613 FDA UDI
Description
QuikClot Bleeding Control Kit, Stanford, OTC, CAT FDA UDI

Identifiers

Catalog Number
0613 FDA UDI
Primary DI / UDI-DI
00841495106132 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Non-organic haemostatic agent FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Non-organic haemostatic agent

QuikClot by Z-Medica, LLC — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-organic haemostatic agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Z-Medica, LLC

Sources (1)

  • FDA UDI 3f66774e-7b90-46f9-b062-8048a2c8eb70 35 fields · synced Jun 8, 2026