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AirWedge

FDA UDI

Class II (US FDA UDI)

by Hovertech International

Identity

Trade Name
AirWedge FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
HoverTech Dual Chamber Inflatable Wedge FDA UDI
Model / Reference
HTPP-200 FDA UDI
Description
HoverTech Dual Chamber Inflatable Wedge FDA UDI

Identifiers

Catalog Number
HTPP-200 FDA UDI
Primary DI / UDI-DI
00816299011388 FDA UDI
510(k) Number
K121287 FDA UDI
FDA Product Code
FNG FDA UDI
GMDN Term
Manual patient lifting belt/harness FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Width — 23 Inch FDA UDI

Category: Manual patient lifting belt/harness

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

Similar devices

Also classified as Manual patient lifting belt/harness.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hovertech International

Sources (1)

  • FDA UDI 34afb934-7921-4bc9-aae0-413ed497b325 38 fields · synced Jun 8, 2026