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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, 2INX5YD FDA UDI
Model / Reference
0131-2S FDA UDI
Description
STERILE COMFO-TEX LATEX FREE ELASTIC BANDAGE, 2INX5YD FDA UDI

Identifiers

Catalog Number
0131-2S FDA UDI
Primary DI / UDI-DI
00614138101548 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
Radiation Sterilization 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

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Manufacturer

Sources (1)

  • FDA UDI 4fe152af-d36b-4c18-9a96-16bd18c31278 35 fields · synced Jun 1, 2026