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Protexer

FDA UDI

Class I (US FDA UDI)

by Icp Medical, Llc

Identity

Trade Name
Protexer FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Procedure Gown, Tested for Chemotherapy Drugs, White, Over the Head, Knit Cuffs, Open Back, Universal FDA UDI
Model / Reference
1 FDA UDI
Description
Procedure Gown, Tested for Chemotherapy Drugs, White, Over the Head, Knit Cuffs, Open Back, Universal FDA UDI

Identifiers

Catalog Number
ICP-7050C FDA UDI
Primary DI / UDI-DI
00813360021550 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Isolation gown, single-use

Protexer by Icp Medical, Llc — 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

Manufacturer
Icp Medical, Llc

Sources (1)

  • FDA UDI ab591922-46e8-4016-bfb7-9cc4b7376ffa 34 fields · synced May 30, 2026