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Medical Boom LP

by Amico Clinical Solutions Corp 56 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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00684706009927 UDI-DI Date14 Oct 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  • Withdrawn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
Medical Boom
Generic Name
Operating room light
Model / Ref / Catalog
LP, LP-HB-N-41
Primary DI / UDI-DI
00684706009927
FDA Product Code
FSY
GMDN Term
Operating room light
Device Class
Class II
Regulation Number
878.4580
GUDID distribution status
In Commercial Distribution

Other devices from Amico Clinical Solutions Corp

See all devices from Amico Clinical Solutions Corp →

Properties

  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (11)

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