← Back to catalogue

Olimax/Wildcat Isolation Gown

FDA UDI

Class I (US FDA UDI)

by Wildcat Ppe, LLC

Identity

Trade Name
Olimax/Wildcat Isolation Gown FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
Non Surgical Disposable Isolation Gown AAMI Level 2 L FDA UDI
Model / Reference
L FDA UDI
Description
Non Surgical Disposable Isolation Gown AAMI Level 2 L FDA UDI

Identifiers

Catalog Number
WPPE0058 FDA UDI
Primary DI / UDI-DI
00860009514102 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Isolation gown, single-use

Olimax/Wildcat Isolation Gown by Wildcat Ppe, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Wildcat Ppe, LLC

Sources (1)

  • FDA UDI eb185433-24b2-4f83-92a6-c8ae929ae53d 34 fields · synced Jun 6, 2026