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ClosureFast

FDA UDI

Class I (US FDA UDI)

by Covidien LP

Identity

Trade Name
ClosureFast FDA UDI
Generic Name
Wound compression dressing FDA UDI
Device Name
Compression Bandages,Cohesive,6"" x 15' (15.24 cm x 4.572 m) FDA UDI
Model / Reference
CB-CO-6 x 5 FDA UDI
Description
Compression Bandages,Cohesive,6"" x 15' (15.24 cm x 4.572 m) FDA UDI

Identifiers

Catalog Number
CB-CO-6 x 5 FDA UDI
Primary DI / UDI-DI
10884521140219 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Wound compression dressing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 6 Inch FDA UDI
Length — 15 Feet FDA UDI

ClosureFast by Covidien LP — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI d7fa5187-71ad-4288-bef6-eecd7cb74a4e 37 fields · synced May 31, 2026