4,101 results · 25ms · Sources: EU EUDAMED, US FDA

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Affinity NT Oxygenator with Cortiva BioActive Surface

FDA 510(k)
FDA Class 2 ·Cardiovascular

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM19001622050161·Rotary instrument für surgical application

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM19001623160161·Rotary instrument für surgical application

Beyes

FDA UDI
Beyes Dental Canada Inc·00990010305069·FG CARBIDE BONE CUTTER 162-016

Straight Trocar Pin 3.2x70

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215061906·

Avalign

FDA UDI
Avalign Technologies, Inc.·00190776020286·Keyhole Bracket

PRECICONTROL CLINCHEM MULTI 1 AND 2

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

RAPID DIGITAL THERMOMETER, MODEL RDT -18 SERIES

FDA 510(k)
FDA Class 2 ·General Hospital

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120214771·Carbide, cone pointed, bone cutter

SSW CARBIDE

FDA UDI
Ss White Burs, Inc.·D690177362·FG CARBIDE BONE CUTTER 162-016 - 5 PACK

SSW CARBIDE

FDA UDI
Ss White Burs, Inc.·D6901773612·FG CARBIDE BONE CUTTER 162-016 - 1 PACK

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120214781·Carbide, cone pointed, bone cutter

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120214751·Carbide, cone pointed, bone cutter

BUSCH®, BNA®

FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120214761·Carbide, cone pointed, bone cutter

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 10, 2014

CD HORIZON LEGACY SPINAL SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·June 11, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 14, 2011

FLANGE FIXTURE AND ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·May 16, 2016

NUCLEUS FREEDOM IMPLANT WITH CONTOUR ADVANCE ELECTRODE

FDA Adverse Event
Injury ·COCHLEAR LTD·Product code MCM·December 15, 2016

NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR LTD.·Product code MCM·May 16, 2016