HoverTech Air Supply

FDA UDI

Class II (US FDA UDI)

by Hovertech International

Identity

Trade Name: HoverTech Air Supply FDA UDI
Generic Name: Medical device air compressor FDA UDI
Device Name: 100V, 50/60Hz HTAIR HoverTech Air Supply FDA UDI
Model / Reference: HTAIR1000 FDA UDI
Description: 100V, 50/60Hz HTAIR HoverTech Air Supply FDA UDI

Identifiers

Catalog Number: HTAIR1000 FDA UDI
Primary DI / UDI-DI: 00816299011227 FDA UDI
FDA Product Code: FRZ FDA UDI
FNG FDA UDI
GMDN Term: Medical device air compressor FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6775 FDA UDI
880.5500 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

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Medical device air compressor

HoverTech Air Supply by Hovertech International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 06bde8ed-3e6a-4679-b743-7a83b7470c7a 36 fields · synced Jun 6, 2026