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

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MIRAGE FULL FACE MASK SERIES 2

FDA 510(k)
FDA Class 2 ·Anesthesiology

24M - PG&E Class A 21 BBP

FDA UDI
Certified Safety Manufacturing, Inc.·00766588233062·PG&E Class A 21 BBP - 24M

Oscar 2, Model 250D

FDA UDI
SUNTECH MEDICAL, INC.·10840935108481·

MINIME NASAL MASK, MODEL P/N 50220

FDA 510(k)
FDA Class 2 ·Anesthesiology

C. DIFFICILE TOX A/B II

FDA 510(k)
FDA Class 1 ·Microbiology

ASR ACETABULAR CUPS 60

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL·Product code KWA·March 27, 2013

DRIVER RX CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code MAF·March 16, 2011

CLEARLINK SYSTEM - TYPE CATH SET/MALE LUER LOCK ADAPTER

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORP.·Product code FPA·April 1, 2008

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PENTAX

FDA Adverse Event
Injury ·PENTAX·Product code EOQ·January 10, 2017

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026

PANEL PHOENIX PMIC-110

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026