Single Patient Use HoverMatt

FDA UDI

Class II (US FDA UDI)

by Hovertech International

Identity

Trade Name: Single Patient Use HoverMatt FDA UDI
Generic Name: Patient transfer system, powered FDA UDI
Device Name: 50" Single Patient Use Air Transfer Mattress: Regard(ROI) FDA UDI
Model / Reference: RGMT50FL-REG FDA UDI
Description: 50" Single Patient Use Air Transfer Mattress: Regard(ROI) FDA UDI

Identifiers

Catalog Number: RGMT50FL-REG FDA UDI
Primary DI / UDI-DI: 00816299012194 FDA UDI
FDA Product Code: FRZ FDA UDI
GMDN Term: Patient transfer system, powered 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Width — 50 Inch FDA UDI

Category: Patient transfer system, powered

Single Patient Use HoverMatt by Hovertech International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient transfer system, powered.

PremierPro Air Transfer Mats — SVS LLC · Class II
PremierPro Air Transfer Mats — SVS LLC · Class II
Sprint 200 — L I N E T spol. s r.o. · Class II
AirDrive Caddie™ — Qfix · Class I
AIR-MATT — AIR-MATT INCORPORATED · Class I
PremierPro Air Transfer Mats — SVS LLC · Class II
AIR-MATT — AIR-MATT INCORPORATED · Class I
AIR-MATT — AIR-MATT INCORPORATED · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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

Manufacturer

Manufacturer: Hovertech International

Sources (1)

FDA UDI 85c8e54d-e0e3-4284-852c-07e5586f20c0 36 fields · synced Jun 1, 2026