54 results
·
20ms
·
Sources: EU EUDAMED, US FDA
DIXI 2
FDA 510(k)
FDA Class 2
·Dental
PowerPICC
FDA UDI
Bard Access Systems, Inc.·00801741101489·Catheter Placement Kit
CUSTOM PROCEDURE KIT
FDA UDI
MEDIVATORS INC.·40677964004627·CUSTOM PROCEDURE KIT
TEWA
FDA UDI
asia-med Gesellschaft für Akupunkturbedarf mbH & Co. KG·04251282502089·TeWa CB-Type 70100 (s): uncoated acupuncture ne...
Brite-Gear
FDA UDI
ORMCO CORPORATION·00889989023541·Facebow SHORT LG 044 YELLOW
GeneXpert Dx System
FDA UDI
CEPHEID·07332940004149·XPERT, GENEXPERT DX SYSTEM
RENAFLO II HF 2000 HEMOFILTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
HARDYDISK, CEFAZOLIN, 30MCG
FDA 510(k)
FDA Class 2
·Microbiology
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/10 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·January 12, 2021
GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/12 MM R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 11, 2022
UNKNOWN CERAMIC HEAD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·August 9, 2017
UNKNOWN CERAMIC HEAD
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code LZO·August 9, 2017
UNKNOWN RINGLOC ARCOM LINER
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017
UNKNOWN M2A RINGLOC LINER
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017
UNKNOWN BI METRIC INTERLOC STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDL·August 8, 2017
UNKNOWN CO CR HEAD
FDA Adverse Event
Malfunction
·BIOMET ORTHOPEDICS·Product code JDI·August 9, 2017
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FKX·March 12, 2013
CAPSURE SENSE
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 24, 2011
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORP.·Product code LGW·February 21, 2008
UNKNOWN BI METRIC INTERLOC STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDG·August 9, 2017