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Celox A

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX A FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Haemostatic Granules in Applicator. Applicator containing 6g haemostatic granules. The device is indicated for temporary traumatic wound treatment to control moderate to severe bleeding. FDA UDI
Model / Reference
FG08832071 FDA UDI
Description
Haemostatic Granules in Applicator. Applicator containing 6g haemostatic granules. The device is indicated for temporary traumatic wound treatment to control moderate to severe bleeding. FDA UDI

Identifiers

Catalog Number
FG08832071 FDA UDI
Primary DI / UDI-DI
15060206630014 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 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 94e26dbd-5c60-439e-826b-8ac492ebe8cb 36 fields · synced May 30, 2026