13 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT
FDA 510(k)
FDA Class 2
·General Hospital
SITE-SCRUB
FDA UDI
Bard Access Systems, Inc.·10801741086943·Site-ScrubTM IPA Device
UniTip Catheter
FDA UDI
Unisensor AG·07640172973721·
ALLTECH ECHOSTAR 1.5 T MR SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
Smile Makers Personal Lubricant
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082407·Screw, polyaxial, Ø 10.0 mm, length 55 mm, not ...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082391·Screw, polyaxial, Ø 10.0 mm, length 50 mm, not ...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082414·Screw, polyaxial, Ø 10.0 mm, length 60 mm, not ...
uCentum™ comprehensive posterior system
FDA UDI
Ulrich GmbH & Co. KG·04052536082384·Screw, polyaxial, Ø 10.0 mm, length 45 mm, not ...
OPTICROSS?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code OBJ·June 18, 2014
FREESTYLE LITE
FDA Adverse Event
Injury
·Product code NBW·October 25, 2010
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·November 12, 2012
XP-XP Tibial Tray - Interlok 71 mm Item # 195755
FDA Enforcement
Class II
·Terminated·Zimmer Biomet, Inc.·September 18, 2019