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HoverJack® Air Patient Lift

EUDAMEDFDA UDI

Class I (EU MDR)

Ref HJ3902TModel Positioning Device

by HoverTech International

Identity

Trade Name
HoverJack® Air Patient Lift EUDAMED
HoverJack FDA UDI
Generic Name
Manual patient lifting belt/harness FDA UDI
Device Name
39" HoverJack FDA UDI
Model / Reference
Positioning Device EUDAMED
HJ3902T EUDAMEDFDA UDI
Description
39" HoverJack FDA UDI

Identifiers

Catalog Number
HJ3902T FDA UDI
Primary DI / UDI-DI
00816299010435 EUDAMEDFDA UDI
Basic UDI-DI
081629901HJSF EUDAMED
510(k) Number
K041503 FDA UDI
FDA Product Code
FNG FDA UDI
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED
GMDN Term
Manual patient lifting belt/harness FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
880.5500 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 — 39 Inch FDA UDI

Category: Device sterilization/disinfection container, reusable

HoverJack® Air Patient Lift by Hovertech International — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000008435
Authorised Representative
Etac Supply Center AB SE-AR-000001601

Sources (2)

  • EUDAMED 0afda751-385d-47c7-a438-b8b2cef5e2c1 61 fields · synced Jun 19, 2026
  • FDA UDI 44f660f4-e51c-4892-9a34-33312bcf3012 38 fields · synced May 30, 2026