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

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RIST Radial Access Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

Intraoral Scan Body V3 SP

FDA UDI
RP - CONEXOES RESTAURADORAS LTDA·07901059074987·

GORNEY SCISSORS

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896055063·GORNEY SCISSORS CURVED BLADES POWER CUT GOLD

OsteoMed

FDA UDI
OSTEOMED LLC·00845694036399·Quick Release Adapter

Reamer

FDA UDI
Treace Medical Concepts, Inc.·00810111225625·Barrel Reamer

CONVERTORS EQUIPMENT DRAPES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

XKNIFE 5

FDA 510(k)
FDA Class 2 ·Radiology

SERVO I

FDA Adverse Event
Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·August 7, 2004

STATVIEW

FDA Adverse Event
Death ·GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·Product code DRT·April 2, 2004

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 3, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·January 12, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 8, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·July 16, 2025

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·March 30, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 11, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 8, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 18, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·April 9, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code IZI·April 22, 2026

AZURION

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·Product code OWB·May 7, 2026