← Back to catalogue

A Plus

FDA UDI

Class I (US FDA UDI)

by A Plus International, Inc

Identity

Trade Name
A Plus FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
Bulk Fenestrated Disposable O.R. Towel , White, Prewashed, Fenestrated 3", 17"X27", Steam Treated, 100 Pc(s)/Polybag, 400Pc(s)/Bale FDA UDI
Model / Reference
1 FDA UDI
Description
Bulk Fenestrated Disposable O.R. Towel , White, Prewashed, Fenestrated 3", 17"X27", Steam Treated, 100 Pc(s)/Polybag, 400Pc(s)/Bale FDA UDI

Identifiers

Catalog Number
FT-1727-3WS FDA UDI
Primary DI / UDI-DI
00683534820179 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical towel

A Plus by A Plus International, 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

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

Manufacturer

Sources (1)

  • FDA UDI 4e4a3a49-5319-44f8-8af1-9e5b0b29d3a8 34 fields · synced May 30, 2026