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Dutex®

FDA UDI

Class I (US FDA UDI)

by Derma Sciences Canada, Inc

Identity

Trade Name
Dutex® FDA UDI
Generic Name
Woven gauze roll/sheet FDA UDI
Device Name
4 in X 4.5 yards, 2 ply, 20X10 mesh gauze 100% cotton sterilized bandage roll. FDA UDI
Model / Reference
77783 FDA UDI
Description
4 in X 4.5 yards, 2 ply, 20X10 mesh gauze 100% cotton sterilized bandage roll. FDA UDI

Identifiers

Catalog Number
DUP77783 FDA UDI
Primary DI / UDI-DI
00809958071410 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze roll/sheet FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 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

No

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

Category: Woven gauze roll/sheet

Dutex® by Derma Sciences Canada, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze roll/sheet.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c5b7e286-9a89-49d4-837d-b9d1de1811c5 36 fields · synced Jun 6, 2026