187 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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