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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 Pad. The device is indicated for temporary external use to control moderate to severe bleeding. The hemostatic gauze is for temporary external use only. FDA UDI
Model / Reference
FG08834281 FDA UDI
Description
Hemostatic Gauze Pad. The device is indicated for temporary external use to control moderate to severe bleeding. The hemostatic gauze is for temporary external use only. FDA UDI

Identifiers

Catalog Number
FG08834281 FDA UDI
Primary DI / UDI-DI
15060206630175 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 — 8 Inch FDA UDI
Width — 8 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 a0a8f030-5e64-42bf-b0da-4d3531293d4a 36 fields · synced Jun 1, 2026