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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

IMPEDIMED - EXTRACELLULAR FLUID ANALYZER MODEL: L-DEX U400

FDA 510(k)
FDA Class 2 ·Cardiovascular

Bur PM2-70 80K Diam Ø4.0 St

FDA UDI
Bien-Air Surgery SA·17630055515039·

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526743588·LEVAMED ANKLE SUPPORT SAND I

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361005766·Arena-L, 38x28, Lordotic 12 degrees, 11H

TruLink

FDA UDI
OSI OPTOELECTRONICS, INC.·00859998006477·SpO2 Foam Sensor Single-Patient Use - Pediatric

PERC-D SPINEWAND

FDA 510(k)
FDA Class 2 ·Orthopedic

NLITE SYSTEM, SLS MODEL NUMBER A00-1025

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

NEONATAL BUBBLE CPAP DUAL HEATED CIRCUIT KIT

FDA Adverse Event
Malfunction ·Product code BZE·March 3, 2021

Widex

FDA UDI
Widex A/S·05706069722604·Widex mind330 M3-X ITE (Clay brown S-330 ) Tele...

Widex

FDA UDI
Widex A/S·05706069724745·Widex D-CIC (Clay brown S-330 ) Right, RC coil

Widex

FDA UDI
Widex A/S·05706069723458·Widex D-XP ITE (Clay brown S-330 ) Telecoil, RC...

Widex

FDA UDI
Widex A/S·05706069725704·Widex EVOKE E-CIC (Clay brown S-330 ) Right, RC...

Widex

FDA UDI
Widex A/S·05706069722970·Widex UNIQUE U-XP ITE (Clay brown S-330 ) Telec...

Widex

FDA UDI
Widex A/S·05706069724387·Widex UNIQUE U-CIC (Clay brown S-330 ) Right, R...

Widex

FDA UDI
Widex A/S·05706069725100·Widex EVOKE E-XP (Clay brown S-330 ) Telecoil, ...

NCB PERIPROSTHETIC FEMUR POLYAXIAL LOCKING PLATE SYSTEM

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code HRS·April 4, 2023

BUBBLE CPAP CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011

BUBBLE CPAP CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZD·April 19, 2011

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 8, 2013

DIAMONDBACK 360 ORBITAL ATHERECTOMY SYSTEM

FDA Adverse Event
Injury ·CARDIOVASCULAR SYSTEMS, INC.·Product code MCW·May 19, 2011