← Back to catalogue

Evacuation HoverJack

FDA UDI

Class II (US FDA UDI)

by Hovertech International

Identity

Trade Name
Evacuation HoverJack FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
32" Hospital Evacuation HoverJack FDA UDI
Model / Reference
HJ32EV FDA UDI
Description
32" Hospital Evacuation HoverJack FDA UDI

Identifiers

Catalog Number
HJ32EV FDA UDI
Primary DI / UDI-DI
00816299010411 FDA UDI
510(k) Number
K041503 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Width — 32 Inch FDA UDI

Category: Manual patient lifting belt/harness

Evacuation HoverJack 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

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

Manufacturer

Manufacturer
Hovertech International

Sources (1)

  • FDA UDI eaddcd4f-cfa5-44f1-8b16-a93077d6d817 38 fields · synced May 30, 2026