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Celox- A Cms

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX- A CMS FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Hemostatic Granules in an Applicator - Indicated for Temporary traumatic wound treatment to control moderate to severe bleeding. For temporary external use only FDA UDI
Model / Reference
FG05832101 FDA UDI
Description
Hemostatic Granules in an Applicator - Indicated for Temporary traumatic wound treatment to control moderate to severe bleeding. For temporary external use only FDA UDI

Identifiers

Catalog Number
30-235 FDA UDI
Primary DI / UDI-DI
15060206630861 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Chitosan haemostatic agent, professional, non-bioabsorbable 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

Dimensions & Sizes

Size
Weight — 6 Gram FDA UDI

Category: Chitosan haemostatic agent, professional, non-bioabsorbable

Celox- A Cms by Medtrade Products , Ltd. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Chitosan haemostatic agent, professional, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 78f3e72c-76b1-48fa-8563-e878e9f1dcfb 36 fields · synced May 30, 2026