← Back to catalogue

Medline Industries, Inc.

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Isolation gown, single-use FDA UDI
Device Name
COVERALL,BRTHBL,EL WRST/ANKL,WHT,2XL FDA UDI
Model / Reference
NONCV940XXL FDA UDI
Description
COVERALL,BRTHBL,EL WRST/ANKL,WHT,2XL FDA UDI

Identifiers

Catalog Number
NONCV940XXL FDA UDI
Primary DI / UDI-DI
40888277180643 FDA UDI
FDA Product Code
LYU 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

No

FDA UDI

Category: Isolation gown, single-use

Medline Industries, Inc. by Medline Industries, 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

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

Manufacturer

Sources (1)

  • FDA UDI fc7f57b3-750a-483e-993a-25b5a4c759c7 35 fields · synced May 29, 2026