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Or Towel Abs

FDA UDI

Class I (US FDA UDI)

by Standard Textile Co., Inc.

Identity

Trade Name
OR TOWEL ABS FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
OR TOWEL ABS 18X30 CEIL IMP HMD 3 OR 4 SIDES FDA UDI
Model / Reference
48541124 FDA UDI
Description
OR TOWEL ABS 18X30 CEIL IMP HMD 3 OR 4 SIDES FDA UDI

Identifiers

Catalog Number
48541124 FDA UDI
Primary DI / UDI-DI
00634916059496 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Surgical towel FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 FDA UDI
Commercial Distribution
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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical towel

Or Towel Abs by Standard Textile Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical towel.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4cdde9a4-4e4c-48a7-bed6-911e515153a3 35 fields · synced May 30, 2026