2,422 results · 35ms · 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.

RD RAINBOW LITE SET-1 NEO ADH

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code QWE·October 6, 2025

RD RAINBOW LITE SET-1 NEO ADH

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code QWE·February 6, 2026

ON-Q C-BLOC: 400ML, 2-14 ML/HR, SAF

FDA Adverse Event
Injury ·I-FLOW LLC·Product code MEB·February 20, 2014

ARNDT AIRWAY EXCHANGE CATHETER SET

FDA Adverse Event
Injury ·COOK INC·Product code LRC·September 28, 2022

Hyperoxia Monitoring Device Adjunct To Pulse Oximetry

FDA classification
FDA Class 2 ·Hyperoxia Monitoring Device Adjunct To Pulse Oximetry

USA Elite

FDA UDI
Gyrus ACMI, LLC·00821925038653·ACMI USA Elite System and USA Series Self Seali...

TWE Meulebeke NV

FDA registration
TWE Meulebeke NV·2 products·🇧🇪 Belgium

GN ReSound

FDA UDI
Gn Hearing A/S·05708296126378·HI,RS VOT950-DWE ITE

GN ReSound

FDA UDI
Gn Hearing A/S·05708296126361·HI,RS VOT930-DWE ITC

TWE Nonwovens US, Inc.

FDA registration
TWE Nonwovens US, Inc.·1 product·🇺🇸 United States

Measles (Rubeola) Antigen Control Slide, 2 wells

FDA UDI
Bion Enterprises, Ltd.·B110QME60020·

Life Support Proucts (LSP)

FDA UDI
Allied Medical, LLC·00026072001134·Resuscitator, LSP, EMT, Swedish, WI Hose Assy. ...

HU-FRIEDY

FDA UDI
HU-FRIEDY MFG. CO., LLC·10889950035051·#23 /QW EXPRO #6 SATIN STEEL HANDLE

QA-ES

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

XIAMEN TWE ORTHOPEDICS CO., LTD

FDA registration
XIAMEN TWE ORTHOPEDICS CO., LTD·9 products·🇨🇳 China

Quasar MED IE (QIE) Limited

FDA registration
Quasar MED IE (QIE) Limited·1 product·🇮🇪 Ireland

L14-5WE Ultrasonic Probe(FDA)

FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904095493·

V11-3WE Ultrasonic Transducer(FDA)

FDA UDI
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.·06944904088112·

QUINTON Q-TE; RMS

FDA 510(k)
FDA Class 2 ·Cardiovascular

TWE DIERDORF GMBH AND CO. KG

FDA registration
TWE DIERDORF GMBH AND CO. KG·1 product·🇩🇪 Germany