← Back to catalogue

Comfo-Tex™

FDA UDI

Class I (US FDA UDI)

by Tetra Medical Supply Corp.

Identity

Trade Name
Comfo-Tex™ FDA UDI
Generic Name
Pressure bandage, non-latex, single-use FDA UDI
Device Name
STERILE COMFO-TEX LATEX FREE ELASTIC BANDAGE, 6INX5YD FDA UDI
Model / Reference
0131-6S FDA UDI
Description
STERILE COMFO-TEX LATEX FREE ELASTIC BANDAGE, 6INX5YD FDA UDI

Identifiers

Catalog Number
0131-6S FDA UDI
Primary DI / UDI-DI
00614138101623 FDA UDI
FDA Product Code
FQM FDA UDI
GMDN Term
Pressure bandage, non-latex, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Pressure bandage, non-latex, single-use

Comfo-Tex™ by Tetra Medical Supply Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pressure bandage, non-latex, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 8d68b594-b9c3-4bc2-b7af-dd23015a1fe1 35 fields · synced May 30, 2026