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Quikclot

FDA UDI

Class U (US FDA UDI)

by Teleflex Incorporated

Identity

Trade Name
QUIKCLOT FDA UDI
Generic Name
Non-organic haemostatic agent FDA UDI
Device Name
QuikClot Interventional, N/Clamshell, N/Tegaderm, Multi-Lang, 10X FDA UDI
Model / Reference
IPN930335 FDA UDI
Description
QuikClot Interventional, N/Clamshell, N/Tegaderm, Multi-Lang, 10X FDA UDI

Identifiers

Catalog Number
467Z FDA UDI
Primary DI / UDI-DI
10841495149594 FDA UDI
FDA Product Code
QSY 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

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
MRI Safety
MR Safe FDA UDI

Category: Non-organic haemostatic agent

Quikclot by Teleflex Incorporated — 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
Teleflex Incorporated

Sources (1)

  • FDA UDI 730f96db-cea1-492c-a006-dd3717c0249d 36 fields · synced May 29, 2026