105 results
·
49ms
·
Sources: EU EUDAMED, US FDA
Custom Surgical GmbH
Manufacturer
🇩🇪 Germany·2 Basic UDI-DIs·4 Devices
CUSTOM SURGICAL GMBH
FDA registration
CUSTOM SURGICAL GMBH·3 products·🇩🇪 Germany
MicroREC
Device
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·On the market
Beamsplitter
Device
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·On the market
Beamsplitter
Device
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·On the market
Beamsplitter
Device
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·On the market
MicroREC
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·1 device
Beamsplitter
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Custom Surgical GmbH·3 devices
LUHR O/SET SCR/DRI 90 DEG
FDA Adverse Event
Malfunction
·HOWMEDICA INC.·Product code HXX·August 11, 1997
MEGA PULSE
FDA Adverse Event
Malfunction
·RICHARD WOLF GMBH·Product code GEX·February 24, 2022
OP-TISCH MARS SELECT DS
FDA Adverse Event
Malfunction
·BAXTER MEDICAL SYSTEMS GMBH + CO. KG·Product code GDC·December 8, 2022
G/K UNIV FREE/H TARGET DEVICE
FDA Adverse Event
Malfunction
·HOWMEDICA INC.·Product code LXH·December 30, 1997
MAQUET LEG HOLDER
FDA Adverse Event
Injury
·Product code FQO·October 24, 2018
COPIOS PERICARDIUM MEMBRANE
FDA Adverse Event
Injury
·TUTOGEN MEDICAL, GMBH·Product code NPL·January 18, 2024
CARDIOHELP
FDA Adverse Event
Death
·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·July 15, 2024
ALLOFT-S ALLOCLASSIC SHL 56/KK
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code KWA·January 15, 2018
HIP MOM IMPLANT
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·May 2, 2017
TIPCONTROL
FDA Adverse Event
Malfunction
·RICHARD WOLF GMBH·Product code HWE·March 1, 2024
SCREW PIN WITH STOP 3,2MM X 30MM
FDA Adverse Event
Malfunction
·IMPLANTCAST GMBH·Product code LXH·January 29, 2026
MOBILELINK ACETABULAR CUP SYSTEM
FDA Adverse Event
Malfunction
·WALDEMAR LINK GMBH & CO. KG·Product code OQG·July 17, 2023