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Celox Ems

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX EMS FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Hemostatic Gauze Pads: The device is indicated for: temporary external use to control moderate to severe bleeding. Hemostatic gauze is for temporary external use only FDA UDI
Model / Reference
FG08834291 FDA UDI
Description
Hemostatic Gauze Pads: The device is indicated for: temporary external use to control moderate to severe bleeding. Hemostatic gauze is for temporary external use only FDA UDI

Identifiers

Catalog Number
FG08834291 FDA UDI
Primary DI / UDI-DI
15060206630168 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 — 4 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Chitosan haemostatic agent, professional, non-bioabsorbable

Celox Ems 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 22f5e5c1-2932-4607-aec9-99ba52d13b46 36 fields · synced May 29, 2026