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UP Stairlift Apex Exclusive

by DeVi-Stairlifts B.V. 2 variants

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08720892974402 UDI-DI Date19 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
UP Stairlift
Generic Name
Stairlift, chair
Model / Ref / Catalog
Apex Exclusive, UPCLR110
Primary DI / UDI-DI
08720892974402
FDA Product Code
PCD
GMDN Term
Stairlift, chair
Device Class
Class II
Regulation Number
890.5150
GUDID distribution status
In Commercial Distribution

Other devices from DeVi-Stairlifts B.V.

Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No