404 results · 102ms · Sources: EU EUDAMED, US FDA

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RICHARD WOLF MEDICAL INSTRUMENTS CORP.

FDA registration
RICHARD WOLF MEDICAL INSTRUMENTS CORP.·30 products·🇺🇸 United States

Hulka Clips

FDA UDI
RICHARD WOLF MEDICAL INSTRUMENTS CORP.·00861523000102·Tubal Occluding Device in a sterile pouch (2 Hu...

PRINCESS

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code FAS·November 9, 2022

BIPOLAR CABLE

FDA Adverse Event
Malfunction ·ERBE GMBH·Product code GEI·March 31, 2015

RICHARD WOLF MEDICAL INSTRUMENTS CORP.

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code FDC·May 1, 2003

RICHARD WOLF MEDICAL INSTRUMENTS CORP.

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS·Product code KNS·May 20, 1998

RONGEUR

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code HTX·December 11, 2014

NA

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GEN·May 25, 2023

SHEATH

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GCJ·October 20, 2014

NA

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GEN·May 25, 2023

ALIGATOR GRASPER

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GCJ·December 19, 2014

3 CHIP HD CAMERA HEAD

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code FET·August 4, 2014

POWER STICK M4

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GEY·November 15, 2023

CABLE, HF, UNIPOLAR

FDA Adverse Event
Injury ·BOWA ELECTRONICS·Product code GEI·January 14, 2015

VIPER

FDA Adverse Event
Malfunction ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code FAJ·July 15, 2025

RIGID GRASPER FORCEPS

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code GEN·July 14, 2022

CABLE, HF, UNIPOLAR

FDA Adverse Event
Malfunction ·BOWA ELECTRONIC·Product code GEI·March 28, 2014

WORKING ELEMENT, S-LINE, BIPOLAR

FDA Adverse Event
Malfunction ·RICHARD WOLF GMBH·Product code FDC·December 17, 2013

SHARK

FDA Adverse Event
Injury ·RICHARD WOLF GMBH·Product code FJL·July 21, 2022

HULKA CLIPS

FDA Adverse Event
Injury ·RICHARD WOLF MEDICAL INSTRUMENTS CORP.·Product code KNH·April 2, 2020