9 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELIMINATOR BALLOON DILATOR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471122963·K-WIRE - SINGLE TROCAR 0.9mm DIA x 150mm
PROXIMATE ILS CIRCULAR STAPLERS
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code KOG·June 13, 2006
MULTIPIEZO PRO, MULTIPIEZO
FDA 510(k)
FDA Class 2
·Dental
PAJUNK TUOHY NEEDLES, QUINCKE NEEDLES, CHIBA NEEDLES & CRAWFORD NEEDLES
FDA 510(k)
FDA Class 2
·Anesthesiology
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS·Product code GEX·January 29, 2013
ADMIN SET. FOR LBL. BLD. DERIVW LL
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MALTA·Product code BRZ·December 29, 2010
12MM/130 DEG TI CANN TROCH FIXATION NAIL 400MM/RIGHT-STER
FDA Adverse Event
Injury
·SYNTHES MONUMENT·Product code HSB·July 17, 2014
FOLYSIL SILICONE CATHETER
FDA Adverse Event
Injury
·COLOPLAST A/S·Product code EZL·March 19, 2025