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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Inflatable patient transfer sliding mattress, reprocessed FDA UDI
Device Name
AIR SHEET,LAT,COMFORT GLIDE, BLEND 40X80 FDA UDI
Model / Reference
MSC60041BL FDA UDI
Description
AIR SHEET,LAT,COMFORT GLIDE, BLEND 40X80 FDA UDI

Identifiers

Catalog Number
MSC60041BL FDA UDI
Primary DI / UDI-DI
10193489021141 FDA UDI
FDA Product Code
FMR FDA UDI
GMDN Term
Inflatable patient transfer sliding mattress, reprocessed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 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

Yes

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: Inflatable patient transfer sliding mattress, reprocessed

Medline by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inflatable patient transfer sliding mattress, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI de2f72f4-e77c-4bf9-b744-a8904482be4f 35 fields · synced Jun 8, 2026