17 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.

SOMATOM Emotion 6/16

FDA 510(k)
FDA Class 2 ·Radiology

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704283372·BABY RIBBON RETRACTOR 6" x 1/2"

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100233·LIEBERMAN ASPIRATING SPECULUM V-WIRE

MaxFuse,VBR, 12 (D) x 14 (W) x 32 (H)

FDA UDI
Pioneer Surgical Technology, Inc.·00846468056261·12 (D) x 14 (W) x 32 (H)

ROCHE ELECSYS TROPONIN T STAT (SHORT TURNAROUND TIME)

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

THERMO SCIENTIFIC CEDIA MULTI-DRUG OFT CALIBRATORS

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·June 20, 2017

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·August 1, 2017

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·July 25, 2017

PENUMBRA SMART COIL

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code HCG·December 11, 2015

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·August 17, 2017

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN·Product code CBK·March 21, 2017

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·October 8, 2014

PRECISION®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 6, 2011

SPRINT FIDELIS

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·June 7, 2013

LOGIC TIBIA PS MOD INSRT SZ 5 11MM

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·June 16, 2023

840 VENTILATOR

FDA Adverse Event
Injury ·COVIDIEN·Product code CBK·June 26, 2017