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Copioumed

FDA UDI

Class I (US FDA UDI)

by Copious International Inc.

Identity

Trade Name
Copioumed FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Copioumed Non-woven apron made of non-woven fabric, widely used in home kitchen conditioning and cleaning, easy to wear, waterproof, oil proof, dust proof. FDA UDI
Model / Reference
APN0X121-1 FDA UDI
Description
Copioumed Non-woven apron made of non-woven fabric, widely used in home kitchen conditioning and cleaning, easy to wear, waterproof, oil proof, dust proof. FDA UDI

Identifiers

Primary DI / UDI-DI
04719882253201 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Isolation 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

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Isolation gown, single-use

Copioumed by Copious International Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Isolation gown, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0f41db04-9a80-4bf6-8b61-701e162f838e 34 fields · synced Jun 8, 2026