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

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EnSite X EP System

FDA 510(k)
FDA Class 2 ·Cardiovascular

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112540·BARRON VACUUM TREPHINE 8.75MM

Rim Plate, Left, 10-Hole, PRS Phoenix

FDA UDI
I.T.S. GmbH·09120069818345·

Rim Plate, Left, 14-Hole, PRS Phoenix

FDA UDI
I.T.S. GmbH·09120069818352·

Votion

FDA UDI
ORTHO TECHNOLOGY, INC.·00190730007612·Votion 018 MC(0T) U/L 5x5 Hks 3, OS Pad U/L 4/5...

K-Y BRAND LIQUIBEADS

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SUPERIOR BATH, MODEL 6300

FDA 510(k)
FDA Class 2 ·Physical Medicine

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·November 7, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 11, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 22, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·October 30, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·October 30, 2023

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 29, 2014

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 8, 2011

TOTAL ASR ACET IMP SIZE 54

FDA Adverse Event
Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 8, 2013

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·October 11, 2023

RAD-97 PULSE CO-OXIMETER WITH NOMOLINE CAPNOGRAPHY

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 12, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 15, 2023

RAD-97 PULSE CO-OXIMETER

FDA Adverse Event
Malfunction ·MASIMO - 15750 ALTON PKWY·Product code MWI·December 5, 2023

BD PLASTICPACK SYRINGE

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·July 22, 2023