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Vancare VanMove

FDA UDI

Class I (US FDA UDI)

by Vancare Inc

Identity

Trade Name
Vancare VanMove FDA UDI
Generic Name
Solid-seat mobile patient lifting system seat FDA UDI
Device Name
Manual Transfer AId. FDA UDI
Model / Reference
VanMove FDA UDI
Description
Manual Transfer AId. FDA UDI

Identifiers

Catalog Number
MFG-4-1-7550 FDA UDI
Primary DI / UDI-DI
00850030758699 FDA UDI
FDA Product Code
FSA FDA UDI
GMDN Term
Solid-seat mobile patient lifting system seat 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: Solid-seat mobile patient lifting system seat

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

Similar devices

Also classified as Solid-seat mobile patient lifting system seat.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vancare Inc

Sources (1)

  • FDA UDI 17482610-d8ec-44dc-b20a-2b20af329b54 34 fields · synced May 29, 2026