← Back to catalogue

Vertical Lifts

FDA UDI

Class II (US FDA UDI)

by Garaventa (Canada) , Ltd.

Identity

Trade Name
Vertical Lifts FDA UDI
Generic Name
Wheelchair/occupant lift FDA UDI
Device Name
Genesis Genesis is a vertical platform wheelchair lift. The Genesis Suitable for commercial or residential projects and can be installed indoors or outdoors. FDA UDI
Model / Reference
01 FDA UDI
Description
Genesis Genesis is a vertical platform wheelchair lift. The Genesis Suitable for commercial or residential projects and can be installed indoors or outdoors. FDA UDI

Identifiers

Primary DI / UDI-DI
B24001 FDA UDI
510(k) Number
K033469 FDA UDI
FDA Product Code
ING FDA UDI
GMDN Term
Wheelchair/occupant lift FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3930 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

Yes

FDA UDI

Category: Wheelchair/occupant lift

Vertical Lifts by Garaventa (Canada) , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair/occupant lift.

Cleared under the same submission

K033469 also covers:

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
Garaventa (Canada) , Ltd.

Sources (1)

  • FDA UDI e43a93f7-3215-4c92-814f-89863bed7a9c 34 fields · synced Jun 8, 2026