culver mobility artemis

by Culver LED Lighting Solution Corp

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00860012388400 UDI-DI	Date18 Jul 2024Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: culver mobility
Generic Name: Electric-motor-driven wheelchair, occupant-controlled
Model / Ref / Catalog: artemis, 20240101

Primary DI / UDI-DI: 00860012388400
FDA Product Code: ITI
GMDN Term: Electric-motor-driven wheelchair, occupant-controlled

Device Class: Class II
Regulation Number: 890.3860
GUDID distribution status: In Commercial Distribution

MRI Safety: MR Unsafe

Properties

Over-the-Counter
Lot / Batch Number
Manufacturing Date

Other properties (11)

Sterile: No
Single Use: No
Implantable: No
Contains Latex: No
Prescription Use: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Expiration Date: No