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CELOX Granules

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX Granules FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Hemostatic Granules: the device is indicated for the local management of bleeding such as lacerations, minor cuts and abrasions. The device is for temporary external use only. FDA UDI
Model / Reference
FG08830441 FDA UDI
Description
Hemostatic Granules: the device is indicated for the local management of bleeding such as lacerations, minor cuts and abrasions. The device is for temporary external use only. FDA UDI

Identifiers

Catalog Number
FG08830441 FDA UDI
Primary DI / UDI-DI
15060206630656 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

No

FDA UDI

Over-the-Counter

Yes

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 — 2 Gram FDA UDI

Category: Chitosan haemostatic agent, professional, non-bioabsorbable

CELOX Granules 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 a2de8ec5-0f78-45b0-bf84-e57b67710e54 36 fields · synced May 31, 2026