110 results · 25ms · Sources: EU EUDAMED, US FDA

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NEUROSTAR TMS THERAPY SYSTEM

FDA 510(k)
FDA Class 2 ·Neurology

N/A

FDA UDI
Tyber Medical, LLC·M695M1302330·

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351115127·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351117381·LAP-Insert only, Ø5mm, l=330mm Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351110658·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351108785·LAP-Instrument, Ø5mm, l=330mm, flushp. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351102578·LAP-Instrument, Ø5mm, l=330mm, flushp. Graspi...

DANmed

FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351112515·LAP-Instrument, Ø5mm, l=330mm, detach. Graspi...

SUDOSCAN

FDA 510(k)
FDA Class 2 ·Neurology

TRAVELSOME STANDARD

FDA 510(k)
FDA Class 2 ·Anesthesiology

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·August 24, 2017

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·August 24, 2017

APPLICAT OUT SHAFT

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code LXH·May 24, 2013

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·September 30, 2014

6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code MGB·June 10, 2011

INSPIRE 6F

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·October 28, 2025

RESERVOIR INSPIRE 8

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·May 8, 2026

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·May 31, 2017

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·March 30, 2017

ADVANCE 18 LP LOW PROFILE BALLOON CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code LIT·July 27, 2017