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Sustainable Technologies

FDA UDI

Class II (US FDA UDI)

by Cardinal Health 200, LLC

Identity

Trade Name
Sustainable Technologies FDA UDI
Generic Name
Inflatable patient transfer sliding mattress, reprocessed FDA UDI
Device Name
Regard HoverMatt® SPU Air Transfer Mattress FDA UDI
Model / Reference
ST-RGMT34HLF-REG FDA UDI
Description
Regard HoverMatt® SPU Air Transfer Mattress FDA UDI

Identifiers

Catalog Number
ST-RGMT34HLF-REG FDA UDI
Primary DI / UDI-DI
10885380203114 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Inflatable patient transfer sliding mattress, reprocessed

Sustainable Technologies by Cardinal Health 200, LLC — 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

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Manufacturer

Manufacturer
Cardinal Health 200, LLC

Sources (1)

  • FDA UDI d2e5126c-6e8a-4429-91aa-1d2e3f1fec33 34 fields · synced Jun 8, 2026