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S5001-0011

by Carilex Medical, Inc.

S5001-0011 is a Class II device made by Carilex Medical, Inc., listed in FDA GUDID since 19 Jun 2025 (UDI-DI 04719873698172), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04719873698172 UDI-DI Date19 Jun 2025ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Electrical assistive bed
Model / reference
S5001-0011
Primary DI / UDI-DI
04719873698172
FDA product code
LLI
GMDN term
Electrical assistive bed
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Electrical assistive bed

Similar devices

Other devices filed under FDA product code LLI (Bed, Therapeutic, Ac-Powered, Adjustable Home-Use).

Other devices from Carilex Medical, Inc.

See all devices from Carilex Medical, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)