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CELOX Gauze

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX Gauze FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Haemostatic Gauze: Haemostatic gauze coated with Celox granules. Device is indicated to control moderate to severe bleeding. For temporary external use only. FDA UDI
Model / Reference
FG08838021 FDA UDI
Description
Haemostatic Gauze: Haemostatic gauze coated with Celox granules. Device is indicated to control moderate to severe bleeding. For temporary external use only. FDA UDI

Identifiers

Catalog Number
FG08838021 FDA UDI
Primary DI / UDI-DI
15060206630151 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
Length — 5 Feet FDA UDI
Width — 3 Inch FDA UDI

Category: Chitosan haemostatic agent, professional, non-bioabsorbable

CELOX Gauze 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 05b20bc1-54f9-44c9-a6a6-05090c492610 36 fields · synced May 30, 2026