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ProGear

FDA UDI

Class I (US FDA UDI)

by Prestige Ameritech

Identity

Trade Name
ProGear FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Dry Shield Fluid Resistant Personal Protection Gown FDA UDI
Model / Reference
GN22010 FDA UDI
Description
Dry Shield Fluid Resistant Personal Protection Gown FDA UDI

Identifiers

Primary DI / UDI-DI
00852212003566 FDA UDI
FDA Product Code
FME FDA UDI
GMDN Term
Isolation gown, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6265 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

No

FDA UDI

Category: Isolation gown, single-use

ProGear by Prestige Ameritech — 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
Prestige Ameritech

Sources (1)

  • FDA UDI 86a03018-8646-4119-9758-61898623e5d3 34 fields · synced Jun 9, 2026