23 results · 23ms · Sources: EU EUDAMED, US FDA

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HD7 DIAGNOSTIC ULTRASOUND SYSTEM

FDA 510(k)
FDA Class 2 ·Radiology

Hillrom™

FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761976214·Trumpf Medical/Medizin Pad Carbon FloatLine G

Pads

FDA UDI
Baxter Medical Systems GmbH + Co. KG·00887761969162·Pad Carbon FloatLine G

iTotal® CR Keel Punch Tip

FDA UDI
Conformis, Inc.·00850268007286·iTotal® CR 14mm Tibial Keel Punch Tip Reusable ...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450181720·

Clamp, Hysterectomy, model Z 35.5cm angled shanks angled

FDA UDI
Geister Medizintechnik GmbH·04057034373439·Clamp, Hysterectomy, model Z 35.5cm...

MODIFICATION TO OPTICAL TRACKING SYSTEM (OTS)

FDA 510(k)
FDA Class 2 ·Neurology

FREE T4 (THYTOXINE) MICROPLATE EIA TEST MODELS # 1225-300

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·April 5, 2024

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES (DBA ANGIOTECH)·Product code GAW·April 3, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·February 12, 2013

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAP·September 16, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·September 23, 2009

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code GAW·May 15, 2008

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Injury ·SURGICAL SPECIALITIES CORP·Product code GAW·February 25, 2014

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code GAW·October 22, 2009

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code OTN·April 26, 2013

LIGHTSPEED VCT

FDA Adverse Event
Injury ·GE MEDICAL SYSTEMS, LLC·Product code JAK·April 22, 2011

HEARTSTART MRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code LDD·July 17, 2008

E-POLY TIBIAL BEARINGS

FDA Adverse Event
Injury ·BIOMET UK LTD.·Product code JWH·July 12, 2017