2,240 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Linvatec SRS PopLok
FDA UDI
Conmed Corporation·20845854014285·POPLOK SUTURE ANCHOR WITH ONE #2 (5 METRIC) HI-...
Linvatec SRS PopLok
FDA UDI
Conmed Corporation·20845854013554·POPLOK SUTURE ANCHOR WITH TWO #0 (3.5 METRIC) H...
Linvatec SRS PopLok
FDA UDI
Conmed Corporation·20845854014117·POPLOK SUTURE ANCHOR WITH ONE #2 (5 METRIC) HI-...
Linvatec SRS PopLok
FDA UDI
Conmed Corporation·20845854013998·POPLOK SUTURE ANCHOR WITH TWO #0 (3.5 METRIC) H...
2.8 MM POPLOK SUTURE ANCHOR
FDA Adverse Event
Malfunction
·CONMED UTICA·Product code MBI·May 29, 2024
LINVATEC SRS POPLOK
FDA Adverse Event
Malfunction
·CONMED·Product code MBI·May 19, 2026
2.8MM POPLOK SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE
FDA Adverse Event
Malfunction
·CONMED·Product code MBI·October 12, 2017
2.8MM POPLOK SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE
FDA Adverse Event
Malfunction
·CONMED·Product code MBI·October 12, 2017
2.8 MM POPLOK SUTURE ANCHOR
FDA Adverse Event
Malfunction
·CONMED UTICA·Product code MBI·May 29, 2024
3.3MM SRS POPLOK, SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code MBI·February 5, 2019
2.8MM POPLOK SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code MBI·September 12, 2018
3.3MM SRS POPLOK, SUTURE ANCHOR WITH ONE NO. 2 (5 METRIC) HI-FI SUTURE
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code MBI·March 16, 2020
ACL TOP 500 CTS
FDA Adverse Event
Malfunction
·INSTRUMENTATION LABORATORY - BEDFORD·Product code GKP·October 7, 2016
BCS(R) XP
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·August 12, 2015
BCS XP
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code GKP·September 9, 2015
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·March 20, 2012
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·March 7, 2012
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·February 15, 2012
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·February 8, 2012
PROTIME MICROCOAGULATION SYSTEM
FDA Adverse Event
Malfunction
·INTERNATIONAL TECHNIDYNE CORP.·Product code GKP·March 13, 2012