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Bracket Pro Serie® 350 – MD 230-12-LP35-MD

by Technimount Medicale Inc GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00628678604148 UDI-DIDate21 Sep 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Bracket Pro Serie® 350 – MD
Generic Name
Portable active medical device mount
Model / Ref / Catalog
230-12-LP35-MD
Primary DI / UDI-DI
00628678604148
FDA Product Code
FOX
GMDN Term
Portable active medical device mount
Device Class
Class I
Regulation Number
880.6990
GUDID distribution status
In Commercial Distribution

Other devices from Technimount Medicale Inc

See all devices from Technimount Medicale Inc →

Properties

  • Premarket Exempt

Other properties (13)

  • 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
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No