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First Aid Only

FDA UDI

Class I (US FDA UDI)

by Acme United Corporation

Identity

Trade Name
First Aid Only FDA UDI
Generic Name
Surgical gown, single-use FDA UDI
Device Name
Gown, medium impervious FDA UDI
Model / Reference
362000 FDA UDI
Description
Gown, medium impervious FDA UDI

Identifiers

Catalog Number
362000 FDA UDI
Primary DI / UDI-DI
00738743007191 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Surgical gown, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical gown, single-use

First Aid Only by Acme United Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e7c3ff2f-a930-45c8-bc9a-93c5ec6c74c1 35 fields · synced Jun 8, 2026