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Vancare VanGo

FDA UDI

Class I (US FDA UDI)

by Vancare Inc

Identity

Trade Name
Vancare VanGo FDA UDI
Generic Name
Mobile patient lifting system, electrically-powered FDA UDI
Device Name
Full body mobile floor lift. Aluminum lift with Intellipac option. Weight capacity 450 lbs. FDA UDI
Model / Reference
VanGo VG450 w/Intellipac FDA UDI
Description
Full body mobile floor lift. Aluminum lift with Intellipac option. Weight capacity 450 lbs. FDA UDI

Identifiers

Catalog Number
MFG-4-3I-0450 FDA UDI
Primary DI / UDI-DI
00850030758729 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Mobile patient lifting system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5510 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Mobile patient lifting system, electrically-powered

Vancare VanGo by Vancare Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Mobile patient lifting system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vancare Inc

Sources (1)

  • FDA UDI 06e54160-092a-472c-8cd3-6504ba6d2867 34 fields · synced Jun 6, 2026