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BIOMET MICROFIXATION, INC devices, product family

by BIOMET MICROFIXATION, INC 6 variants Basic UDI-DI 889024Z2K4

Shared by every variant

Manufacturer
BIOMET MICROFIXATION, INC(6)
Basic UDI-DI
889024Z2K4
Risk class
Class IIClass I (varies)
Legislation
—
EMDN category
—
Market status
6 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 889024Z2K4.

Recalls

1 recall · FDA

  • Z-1220-2017 Class II · terminated · 10 Jan 2017
    The identification of the devices was non-conforming with off-centered slots and the no-go gage starting in the pilot hole.

Recalls matched to the 6 devices listed on this page; other pages of the family can carry others.

Variants

6 devices · page 1 of 1

Variants of BIOMET MICROFIXATION, INC devices, Basic UDI-DI 889024Z2K4
UDI-DISize and differences
"1.5MM" SYSTEM 01-7167 01-7167 / 01-716700841036013288 —On the market
"2.0/2.4MM" FRACTURE SYSTEM 01-9728 01-9728 / 01-972800841036018443 —On the market
"2.0MM" SYSTEM 01-9070 01-9070 / 01-907000841036016753 —On the market
1.0MM SYSTEM 01-7460 01-7460 / 01-746000841036014346 —On the market
1.0MM/1.5MM SYSTEM 01-7172 01-7172 / 01-717200841036013325 —On the market
1.0MM/1.5MM SYSTEM 01-7465 01-7465 / 01-746500841036014353 —On the market