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Endoscopy trolley monitor arm JESTMA

by Joimax, Inc.

Listed FDA GUDID listing, not in commercial distribution

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 Number04056634001674 UDI-DI Date16 Jan 2023ListedStatusListed GUDID: not 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  • Withdrawn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
Endoscopy trolley monitor arm
Generic Name
Medical monitor/light mount
Model / Ref / Catalog
JESTMA
Primary DI / UDI-DI
04056634001674
FDA Product Code
BZN
GMDN Term
Medical monitor/light mount
Device Class
Class I
Regulation Number
868.6175
GUDID distribution status
Not in Commercial Distribution

Other devices from Joimax, Inc.

See all devices from Joimax, Inc. →

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

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