← Back to catalogue

Cardinal Health

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
CARDINAL HEALTH FDA UDI
Generic Name
Inflatable patient transfer sliding mattress, reprocessed FDA UDI
Device Name
Hovertech Hovermatt Lateral Transfer Mattress FDA UDI
Model / Reference
ST-HM39SPU-HLF-B FDA UDI
Description
Hovertech Hovermatt Lateral Transfer Mattress FDA UDI

Identifiers

Catalog Number
ST-HM39SPU-HLF-B FDA UDI
Primary DI / UDI-DI
10885380168512 FDA UDI
FDA Product Code
FRZ FDA UDI
GMDN Term
Inflatable patient transfer sliding mattress, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6775 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Inflatable patient transfer sliding mattress, reprocessed

Cardinal Health by Cardinalhealth — Class II — 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

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

Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 80b8cf67-a2f7-46c0-8a75-944ef1d1c3d2 34 fields · synced May 30, 2026