← Back to catalogue

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: Non-woven Gauze coated with Celox haemostatic granules. Device is indicated to control moderate to severe bleeding. For temporary external use only. FDA UDI
Model / Reference
FG08838011 FDA UDI
Description
Haemostatic Gauze: Non-woven Gauze coated with Celox haemostatic granules. Device is indicated to control moderate to severe bleeding. For temporary external use only. FDA UDI

Identifiers

Catalog Number
FG08838011 FDA UDI
Primary DI / UDI-DI
15060206630038 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 — 10 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI ad354ab9-6927-4687-9862-2bd4725076bb 36 fields · synced May 30, 2026