SizeWise Matt

FDA UDI

Class II (US FDA UDI)

by Hovertech International

Identity

Trade Name: SizeWise Matt FDA UDI
Generic Name: Patient transfer system, powered FDA UDI
Device Name: 39" SizeWise Transfer Matt FDA UDI
Model / Reference: SW39HS FDA UDI
Description: 39" SizeWise Transfer Matt FDA UDI

Identifiers

Catalog Number: SW39HS FDA UDI
Primary DI / UDI-DI: 00816299010145 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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Width — 39 Inch FDA UDI

Category: Patient transfer system, powered

SizeWise Matt by Hovertech International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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

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Manufacturer

Manufacturer: Hovertech International

Sources (1)

FDA UDI d09850cf-75ca-4556-a164-8cbbd9e9e1ff 37 fields · synced May 30, 2026