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Copioumed

FDA UDI

Class I (US FDA UDI)

by Copioumed International Inc.

Identity

Trade Name
Copioumed FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Copioumed Heavy-Polyethylene Impervious Cover Gown with Thumb Loops offers excellent protection against liquids and fluid exposure in infective wards, the ICU and emergency care. Each is a single-use over-the-head-style gown. FDA UDI
Model / Reference
PEN1B103-1 FDA UDI
Description
Copioumed Heavy-Polyethylene Impervious Cover Gown with Thumb Loops offers excellent protection against liquids and fluid exposure in infective wards, the ICU and emergency care. Each is a single-use over-the-head-style gown. FDA UDI

Identifiers

Primary DI / UDI-DI
04719882250552 FDA UDI
FDA Product Code
OEA 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Isolation gown, single-use

Copioumed by Copioumed 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 99c08bf7-8aeb-4dee-8b17-695f5edae893 34 fields · synced May 30, 2026