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Precaution/Isolation Gown

FDA UDI

Class I (US FDA UDI)

by Standard Textile Co., Inc.

Identity

Trade Name
Precaution/Isolation Gown FDA UDI
Generic Name
Isolation gown, reusable FDA UDI
Device Name
PRECAUTION GOWN GENERIC YELLOW KAUM XL RM (98-8435) USE: 66649995 FDA UDI
Model / Reference
666Y9595 FDA UDI
Description
PRECAUTION GOWN GENERIC YELLOW KAUM XL RM (98-8435) USE: 66649995 FDA UDI

Identifiers

Catalog Number
666Y9595 FDA UDI
Primary DI / UDI-DI
00634916339321 FDA UDI
FDA Product Code
OEA FDA UDI
GMDN Term
Isolation gown, reusable 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

No

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, reusable

Precaution/Isolation Gown by Standard Textile Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Isolation gown, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e50ab7d-aa93-4d98-b0ec-0b0898db0157 35 fields · synced May 30, 2026