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Cerclage Button 3.5T MDS110302C

by Miami Device Solutions

Cerclage Button 3.5T MDS110302C is a Class II device made by Miami Device Solutions, listed in FDA GUDID since 17 May 2018 (UDI-DI 10812269023150), 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 Number10812269023150 UDI-DI Date17 May 2018ListedStatusListed 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  • Withdrawn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

Trade name
Cerclage Button 3.5T
Generic name
Internal orthopaedic fixation system, cerclage wire/cable, non-sterile
Model / Ref / Catalog
MDS110302C
Primary DI / UDI-DI
10812269023150
FDA product code
HWC, HRS
GMDN term
Internal orthopaedic fixation system, cerclage wire/cable, non-sterile
Device class
Class II
Regulation number
888.3040, 888.3030
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterileInternal orthopaedic fixation system, cerclage wire/cable, non-sterile

Other devices from Miami Device Solutions

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Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)