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

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Tornier Perform Humeral System – Stemless

FDA 510(k)
FDA Class 2 ·Orthopedic

ambIT* Introducer - Beveled Tip, Peelable Sheath

FDA UDI
Avanos Medical, Inc.·00193494000615·ambIT* Introducer - Beveled Tip, Peelable Sheath

ambIT

FDA UDI
SUMMIT MEDICAL PRODUCTS, INC.·00857595005022·Introducer- 8 inch

APEX PS Knee

FDA UDI
Omni Life Science, Inc.·00841690113263·PS Insert, Size 4 x 18mm

NA

FDA UDI
Stryker Leibinger GmbH & Co. KG·34546540355653·Bone Screws, Cross-Pin

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220418070·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220418000·

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B1676220418150·

ELECTROSUGRICAL RESECTION AND VAPORIZATION ELECTRODE SERIES

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

GO MEDICAL PATIENT CONTROLLED ANALGESIA DEVICES

FDA 510(k)
FDA Class 2 ·General Hospital

VERSACROSS CONNECT LAAC ACCESS SOLUTION

FDA Adverse Event
Injury ·BAYLIS MEDICAL COMPANY INC.·Product code DRE·April 6, 2023

HF-RESECTION ELECTRODE, FOR TURIS

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·February 9, 2023

HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.2 WIRE, MEDIUM, 12°

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·September 4, 2024

CAPIO OPEN ACCESS SUTURE CAPTURING DEVICE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FHQ·October 31, 2008

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 23, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

HF-RESECTION ELECTRODE, LOOP

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·March 28, 2023

HF-RESECTION ELECTRODE

FDA Adverse Event
Injury ·OLYMPUS WINTER & IBE GMBH·Product code FAS·December 28, 2022

HF-RESECTION ELECTRODE, LOOP

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code FAS·April 27, 2023

BD RAPID DETECTION OF SARS-COV-2 VERITOR

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QKP·November 6, 2020