301 results · 31ms · Sources: EU EUDAMED, US FDA

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OMNI Anseris Hip Stem

FDA 510(k)
FDA Class 2 ·Orthopedic

KMEDIC

FDA UDI
TELEFLEX INCORPORATED·24026704292787·

Novo Surgical

FDA UDI
NOVO SURGICAL, INC.·G586G1711560·dressing forceps, standard pattern, serrated ha...

AUTOMATED IN VITRO QUANTITATIVE ASSAY FOR THE MEASUREMENT OF ALLERGEN SPECIFIC IGE ANTIBODIES

FDA 510(k)
FDA Class 2 ·Immunology

SOUNMED SD-2000 PLUS PORTABLE ULTRASOUND SCANNER

FDA 510(k)
FDA Class 2 ·Radiology

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 14, 2013

LEGEND XT 2CH COMBO

FDA Adverse Event
Injury ·CHATTANOOGA GROUP·Product code IMG·September 23, 2008

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·June 30, 2011

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 29, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 28, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 30, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 24, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·August 5, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·June 29, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EOB·October 22, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·July 30, 2021

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·February 27, 2023

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·December 21, 2022

PENTAX

FDA Adverse Event
Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code PEA·October 7, 2022