152 results · 55ms · Sources: EU EUDAMED, US FDA

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UNITED BIOTECH

FDA registration
UNITED BIOTECH·1 product·🇺🇸 United States

BIOTECH'S IGE IMMUNO RESPONSE TEST ISOTOPE UNIT

FDA 510(k)
FDA Class 2 ·Immunology

KANGAROO

FDA Adverse Event
Malfunction ·COVIDIEN·Product code LZH·February 23, 2018

RESPIRONICS

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, LLC·Product code MNT·May 16, 2022

KARL STORZ

FDA Adverse Event
Other ·KARL STORZ GMBH & CO. KG·Product code LQS·October 12, 2007

CALSTRUX (TRICALCIUM PHOSPHATE)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 13, 2009

OP-1 IMPLANT (OSTEOGENIC PROTEIN 1)

FDA Adverse Event
Injury ·Product code MPY·July 25, 2008

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 25, 2019

CALSTRUX (TRICALCIUM PHOSPHATE)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 13, 2009

CALSTRUX (TRICALCIUM PHOSPHATE)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 13, 2009

BIRTCHER ESU PENCIL

FDA Adverse Event
Injury ·CONMED CORPORATION·Product code GEI·December 1, 1998

OP-1 PUTTY (OSTEOGENIC PROTEIN 1)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 30, 2007

GENADYNE A4 NEGATIVE PRESSURE WOUND THERAPY UNIT

FDA Adverse Event
Malfunction ·GENADYNE BIOTECH, INC·Product code OMP·October 8, 2013

GENERATOR PULSAR REFURBISHED

FDA Adverse Event
Malfunction ·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·December 15, 2014

9610617-2007-00027

FDA Adverse Event
Other ·Product code LQS·October 12, 2007

CALSTRUX (TRICALCIUM PHOSPHATE)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 13, 2009

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 25, 2019

OPTIFLUX 180 NR DIALYZER

FDA Adverse Event
Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·November 9, 2009

CALSTRUX (TRICALCIUM PHOSPHATE)

FDA Adverse Event
Injury ·STRYKER BIOTECH·Product code MPY·July 13, 2009

LOGIQ BOOK ULTRASOUND SCANNER DIAGNOSTIC W/O AC/DC CORD

FDA Adverse Event
Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code ITX·February 12, 2007