778 results · 31ms · Sources: EU EUDAMED, US FDA

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AMG PMP Pediatric

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814695·GENUMEDI SILVER SIZE VI

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112755·BARRON VACUUM PUNCH 7.5MM

24M - Salt River Project-21 - Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588022017·24M - Salt River Project-21 - Metal

36M - Salt River Project-31 - Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588022024·36M - Salt River Project-31 - Metal

JENSEN GOLD FOIL

FDA 510(k)
FDA Class 2 ·Dental

HI-TORQUE WHISPER LS GUIDE WIRE WITH HYDROCOAT HYDROPHILIC COATING, HI-TORQUE WHISPER MS GUIDE WIRE WITH HYDROCOAT HYDRO

FDA 510(k)
FDA Class 2 ·Cardiovascular

IFUSE IMPLANT SYSTEM

FDA Adverse Event
Injury ·SI-BONE, INC.·Product code OUR·November 9, 2017

IFUSE IMPLANT SYSTEM

FDA Adverse Event
Injury ·SI-BONE, INC.·Product code OUR·November 4, 2019

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·June 17, 2022

670G INSULIN PUMP MMT-1780KL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 8, 2022

EVERSENSE SENSOR

FDA Adverse Event
Injury ·SENSEONICS INC.·Product code QCD·February 21, 2024

REPLY

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA S.R.L.·Product code NVZ·June 28, 2013

VENTURE DELUXE WHEELCHAIR

FDA Adverse Event
Death ·TUFFCARE INC·Product code IOR·October 14, 2008

ACUSNARE POLYPECTOMY SNARE

FDA Adverse Event
Injury ·WILSON-COOK MEDICAL INC·Product code KNS·August 4, 2011

DREAMSTATION AUTO BIPAP

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·May 20, 2022

GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 2+ L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 17, 2020

DREAMSTATION AUTO BIPAP

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·June 15, 2022

REMSTAR AUTO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·May 26, 2022

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·June 10, 2022