74 results · 30ms · Sources: EU EUDAMED, US FDA

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IMPEDIMED EXTRA CELLULAR FLUID ANALYSIS, MODEL L-DEX U400

FDA 510(k)
FDA Class 2 ·Cardiovascular

X-Box

FDA UDI
INNO Holdings, Inc.·M71190808250·PEEK, Ta

CoRoent

FDA UDI
Nuvasive, Inc.·00887517283412·CoRoent® LO Ti, 8x10x25mm 5°

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014607702·STERIS-AMSCO 1080, 2080 3.25" DELUXE GEL

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197541411·RZ Tebbet Breast Retractor 80x25m...

MEDLINE STERISET STERILIZATION CONTAINER

FDA 510(k)
FDA Class 2 ·General Hospital

4F-7F MEDI-DYNE TORQ FLOW XLB ANGIOGRAPHIC CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·July 20, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·October 9, 2009

FAST1 INTRAOSSEOUS INFUSION SYSTEM

FDA Adverse Event
Other ·PYNG MEDICAL CORP.·Product code FMI·June 10, 2009

COCR FEMORAL BALL HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JDI·July 23, 2025

MASTERLOC CEMENTLESS TI COATED STD STEM SIZE 4

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 29, 2018

SPIRAL BLADE AIMING ARM FOR TI CANNULATED HUMERAL NAILS-EX

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code LXH·April 26, 2013

HEART START XL

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·August 25, 2014

30327 12CC 100 UNIT HEP SYR {CAN} (5CC)

FDA Adverse Event
Malfunction ·TYCO HEALTHCARE / KENDALL·Product code NZW·July 23, 2008

LINER: MPACT FLAT PE HC 36/E

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·May 5, 2021

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019