634 results · 22ms · 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.

Nitrile Powder Free Examination Glove, Blue Tested for Use with 32 Chemotherapy Drugs and Fentanyl Permeation Resistance Claim

FDA 510(k)
FDA Class 1 ·General Hospital

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772344116·PROTECT.PRO ACTION BACK SUPPORT BLACK M

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112588·BARRON CORNEAL PUNCH 6.75MM

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM

HDI 5000 ULTRASOUND SYSTEM WITH EXTENDED FIELD OF VIEW IMAGING

FDA 510(k)
FDA Class 2 ·Radiology

TITAN MICRO CATHETER, MODEL 105-5074-153; HD INJECTOR, MODEL 103-0305

FDA 510(k)
FDA Class 2 ·Cardiovascular

PERMANENT PACEMAKER ELECTRODE

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL·Product code DTB·August 12, 2023

INTIMA-II Y 22GAX1.00IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 13, 2021

640G INSULIN PUMP MMT-1711K

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 21, 2022

INTIMA-II Y 24GAX0.75IN PRN/EC SLM

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 13, 2021

SERVO-I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·April 8, 2020

630G INSULIN PUMP MMT-1715K 630G BLACK MG

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·February 16, 2022

JAZZY SELECT

FDA Adverse Event
Injury ·Product code INI·October 6, 2008

INFINITI VISION SYSTEM OZIL

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 27, 2013

UNKNOWN OPTEASE VENA CAVA FILTER

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code DTK·August 11, 2011

CAMLOG SCREW LINE IMPLANT PROMOTE PLUS

FDA Adverse Event
Injury ·ALTATEC GMBH·Product code DZE·May 12, 2021

CAMLOG SCREW LINE IMPLANT PROMOTE PLUS

FDA Adverse Event
Injury ·ALTATEC GMBH·Product code DZE·May 12, 2021

CAMLOG SCREW LINE IMPLANT PROMOTE PLUS

FDA Adverse Event
Injury ·ALTATEC GMBH·Product code DZE·May 12, 2021

CAMLOG SCREW LINE IMPLANT

FDA Adverse Event
Injury ·ALTATEC GMBH·Product code DZE·May 12, 2021