27 results · 23ms · 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.

Magic Torque DLVR Guidewire

FDA 510(k)
FDA Class 2 ·Cardiovascular

Monoject

FDA UDI
Cardinal Health, Inc.·10884521544666·Hypodermic Safety Needle

Monoject

FDA UDI
Cardinal Health 200, LLC·10192253025057·Hypodermic Safety Needle 23G x 1.5 in. (0.6 x 3...

AVANOS

FDA UDI
Avanos Medical, Inc.·00193493935048·AVANOS* Single-Shot Epidural Trays

PROPELLER HEAD SCREW SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304269866·

Halyard

FDA UDI
Avanos Medical, Inc.·10680651935042·HYH,EP TRY,S-SHOT,-,-,10

BI-METRIC X-SERIES HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304183094·

EC50 MICRO+ SMOKERLYZER

FDA 510(k)
FDA Class 2 ·Anesthesiology

STAXX XDL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

I-STAT EC4+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

I-STAT EC4+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

I-STAT EC4+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

I-STAT EC4+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

I-STAT EC4+ CARTRIDGE

FDA Adverse Event
Malfunction ·ABBOTT POINT OF CARE·Product code JGS·October 9, 2019

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 10, 2013

ACTIVA PC

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·July 11, 2011

CS100

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·September 30, 2008

INTERCHANGEABLE ULNAR ASSEMBLY

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDC·October 22, 2019

MENTOR CPX4 WITH SUTURE TABS, TALL HEIGHT, SMOOTH

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code LCJ·October 24, 2019

MENTOR CPX4 WITH SUTURE TABS, MED HEIGHT, SMOOTH

FDA Adverse Event
Injury ·MENTOR TEXAS·Product code LCJ·January 10, 2020