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SurgiCount

FDA UDI

Class I (US FDA UDI)

by A Plus International, Inc

Identity

Trade Name
SurgiCount FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
OR Towel, Green, Prewashed, Data Matrix Label, Master Tagged, Banded in 2's, X-Ray, 400 Pcs/Cs FDA UDI
Model / Reference
1 FDA UDI
Description
OR Towel, Green, Prewashed, Data Matrix Label, Master Tagged, Banded in 2's, X-Ray, 400 Pcs/Cs FDA UDI

Identifiers

Catalog Number
C-0603-260-020 FDA UDI
Primary DI / UDI-DI
00683534870242 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical towel

SurgiCount 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

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Manufacturer

Sources (1)

  • FDA UDI 1872336e-7eb2-452e-ad87-a1d58f7e7dc7 34 fields · synced May 30, 2026