9 results · 18ms · Sources: EU EUDAMED, US FDA

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TP 1

FDA 510(k)
FDA Class 3 ·Cardiovascular

DIGI-X

FDA 510(k)
FDA Class 1 ·Radiology

NOVOBIOCIN DISC

FDA 510(k)
FDA Class 1 ·Microbiology

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2014

900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 5, 2012

TRUERESULT

FDA Adverse Event
Malfunction ·NIPRO DIAGNOSTICS, INC.·Product code NBW·June 11, 2015

CERENOVUS CEREBASE DA Guide Sheath, Part Numbers: a) GS9080SD; b) GS9090SD; c) GS9095SD; Vascular guide-catheter, single-use

FDA Recall
Open, Classified ·Medos International Sarl Chemin Blanc 36 Le Locle Switzerland·Product code QJP·February 2, 2024

OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (10 mm diameter) Model: LTF-S190-10 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities, including female reproductive organs.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code HET·November 20, 2023

OLYMPUS ENDOEYE FLEX DEFLECTABLE VIDEOSCOPE (5.4 mm diameter) Model: LTF-S190-5 Used with a video system center, light source, documentation equipment, monitor, hand instruments, electrosurgical unit, and other ancillary equipment for endoscopy and endoscopic surgery within the thoracic and abdominal cavities, including female reproductive organs.

FDA Recall
Open, Classified ·Olympus Corporation of the Americas·Product code HET·November 20, 2023