60 results · 25ms · Sources: EU EUDAMED, US FDA

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ETEST Plazomicin (PLZ) (0.016-256 µg/mL)

FDA 510(k)
FDA Class 2 ·Microbiology

ReLine

FDA UDI
Nuvasive, Inc.·00195377047519·RELINE-O Trial, 8mm H Offset Right L-pop

Pantheon System

FDA UDI
ADLER ORTHO SPA·08050880237692·Pantheon Salvage Cementless Stem L 115 Ø 12

PED. VHS VARI-ANGLE HIP SCREW

FDA UDI
Biomet Orthopedics, LLC·00880304279681·

Zavation

FDA UDI
Zavation LLC·00842166131682·Ti3Z CIF 12mmx14mmx12mm -5 deg

METZENBAUM SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055209·METZENBAUM SCISSORS DELICATE CURVED TUNGSTEN CA...

My Medical

FDA UDI
My Medical Store LLC·G4252005120·Rhinoplasty Rasp, Curved

Marina Medical

FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306805561·Preservation Rhinoplasty: 3mm Rasp, Curved

A-CIFT® SoloFuse®

FDA UDI
SPINEFRONTIER, INC.·00190361021391·A-CIFT SoloFuse 4.2 Screw, Lag, 12mm

CADD® CADD®-SOLIS VIP AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·November 1, 2018

OSCILLOMITT, MODELS CM 1050, CM 1040, CM 1030, CM 1020, CM 1010

FDA 510(k)
FDA Class 2 ·Cardiovascular

MTI ST#1 SILICONE PESSARY

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

CADD-SOLIS VIP AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·June 6, 2019

CADD SOLIS VIP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC·Product code FRN·March 8, 2020

COATED VICRYL (POLYGLACTIN 910) SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAM·January 13, 2006

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·December 16, 2020

CADD-SOLIS VIP AMBULATORY INFUSION PUMP

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FRN·August 23, 2022

TANDEM T:SLIM INSULIN DELIVERY SYSTEM

FDA Adverse Event
Injury ·TANDEM DIABETES CARE·Product code LZG·August 5, 2016

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·November 22, 2019

MONOCRYL POLIGLECAPRONE 25 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAN·November 22, 2019