99 results · 21ms · Sources: EU EUDAMED, US FDA

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NON-CONTACT INFRARED THERMOMETER

FDA 510(k)
FDA Class 2 ·General Hospital

Integra® Jarit®

FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780378297·Integra® Jarit® Adson Forceps, 4-3/4", Extra De...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450242421·

N/A

FDA UDI
Tyber Medical, LLC·M695M1302310·

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384335830·5 pieces

DM

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384335837·5 pieces

CORONARY ARTERY PERFUSION CANNULA WITH SELF-INFLATING BALLOON

FDA 510(k)
FDA Class 2 ·Cardiovascular

KYPHON INFLATION SYRINGE

FDA 510(k)
FDA Class 2 ·Orthopedic

Widex

FDA UDI
Widex A/S·05706069908121·WIDEX MOMENT MRB2D DEMO (Silver Grey ) 330, Tel...

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·06975384337070·6 pieces

KP

FDA UDI
Guilin Kevin Peter Technology Co., Ltd.·16975384337077·6 pieces

SPECTRA WAVEWRITER?

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 19, 2025

AEQ REV II GLENOID BASEPLATE DIA 25MM LONG POST

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code PHX·January 5, 2026

AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·April 18, 2023

AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·April 20, 2023

UNIVERSAL AO REAMER ATTACHMENT 250 RPM

FDA Adverse Event
Malfunction ·ZIMMER SURGICAL S.A.·Product code HTO·May 22, 2013

SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·September 30, 2014

KAPPA 700 DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code DXY·June 16, 2011

AEQ REV II GLENOID BASEPLATE DIA 25MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·December 22, 2023

AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·April 14, 2026