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AllCare, INC

FDA UDI

Class I (US FDA UDI)

by Allcare, Inc.

Identity

Trade Name
AllCare, INC FDA UDI
Generic Name
Surgical towel FDA UDI
Device Name
OR TOWEL, BLUE, COTTON, PRE-WASHED, NON-STERILE, 400/CASE FDA UDI
Model / Reference
ORB-400 FDA UDI
Description
OR TOWEL, BLUE, COTTON, PRE-WASHED, NON-STERILE, 400/CASE FDA UDI

Identifiers

Catalog Number
ORB-400 FDA UDI
Primary DI / UDI-DI
00182921000014 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

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

Yes

FDA UDI

Category: Surgical towel

AllCare, INC by Allcare, 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

Manufacturer
Allcare, Inc.

Sources (1)

  • FDA UDI c1668075-2e23-4864-ad1d-039b8e455b8a 36 fields · synced May 30, 2026