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CELOX Rapid Ribbon - CMS

FDA UDI

Class U (US FDA UDI)

by Medtrade Products , Ltd.

Identity

Trade Name
CELOX Rapid Ribbon - CMS FDA UDI
Generic Name
Chitosan haemostatic agent, professional, non-bioabsorbable FDA UDI
Device Name
Hemostatic Z-Fold Gauze - indicated to control moderate to severe bleeding. For emergency temporary external use only. FDA UDI
Model / Reference
FG05839141 FDA UDI
Description
Hemostatic Z-Fold Gauze - indicated to control moderate to severe bleeding. For emergency temporary external use only. FDA UDI

Identifiers

Catalog Number
30-223 FDA UDI
Primary DI / UDI-DI
15060206630847 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 — 5 Feet FDA UDI
Width — 1 Inch FDA UDI

Category: Chitosan haemostatic agent, professional, non-bioabsorbable

CELOX Rapid Ribbon - CMS 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 08d55641-4b61-4608-8add-fd6450293d90 36 fields · synced Jun 8, 2026