24 results · 21ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

VERIFY SELF-CONTAINED BIOLOGICAL INDICATOR FOR VAPORIZED (VH2O2) STERILIZATION PROCESSES

FDA 510(k)
FDA Class 2 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526827868·***DISC*LEVAMED ANKLE SUPPORT BLACK IV

LEONE SPA

FDA UDI
LEONE SPA·08033707065890·EXTRAORAL ELASTICS 3/8" 14 oz

Symmetry Surgical

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482038703·Symmetry® Probe, Double-Ended, Stainless Steel,...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450212592·

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014

HNM MEDICAL

FDA UDI
HNM STAINLESS, LLC.·00842962108734·00842962108734 HNM-1-09-0514 PROBE, 5 1/2", DOU...

PULPDENT GLAZE II

FDA 510(k)
FDA Class 2 ·Dental

RUMBAR DRAINAGE SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

VKMO 78000 3 QUADROX-I HMO 70000+VHK7000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015

VKMO 78000 #QUADROX-I HMO 70000+VHK7000

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·February 25, 2015

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 20, 2014

BE-VKMO 70000 #QUADR-I HMO70000+VHK7100

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

BE-VKMO 70000 #QUAD-I HMO70000+VHK7100

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

BE-VKMO 70000 #QUADR-I HMO70000+VHK7100

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

HLM TUBING SET W/SOFTLINE COATING

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DWF·April 6, 2016

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 9, 2018

BE-VEMO 7000 #QUADR-I HMO70000+VHK7100

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY AG·Product code DTZ·January 5, 2015

SENSOR?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code EZB·May 2, 2013

BATTERY CAP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·September 15, 2014