12 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Wet Essential95 Personal Lubricant
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ambIT
FDA UDI
SUMMIT MEDICAL PRODUCTS, INC.·00857595005817·PreSet PCA Pump - Green
ambIT* PreSet* PCA Pump
FDA UDI
Avanos Medical, Inc.·00193494000684·PreSet* *PCA Pump
TriVerse Femoral Sizer Paddles
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215097332·
MEDSTAR SYSTEM, MODELS 533-300
FDA 510(k)
FDA Class 2
·Cardiovascular
VisualEyes
FDA 510(k)
FDA Class 2
·Neurology
PREMICATH NEONATAL PICC
FDA Adverse Event
Malfunction
·VYGON GMBH.·Product code LJS·August 6, 2014
AC POWER MODULE
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·July 18, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
BD CATHENA¿ SAFETY IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021
Sure T, contact, contact detach, neria, neria detach, neria multi and thalaset Used in combination with infusion pumps for continuous subcutaneous infusion of medication.
FDA Enforcement
Class II
·Terminated·Unomedical As·July 1, 2015