30 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ULTRASONIC NEBULIZER (MESH TYPE)
FDA 510(k)
FDA Class 2
·Anesthesiology
SMARTPIN
FDA UDI
Conmed Corporation·10845854012369·SMARTPIN SELF-REINFORCED TECHNOLOGY, Ø 1.5 X 20 MM
DD tempMED
FDA UDI
Dental Direkt GmbH·EDDIK115201·DD tempMED are pre-colored dental milling blank...
SMARTPIN
FDA UDI
Conmed Corporation·10845854012366·SMART PIN, DIAMETER 1.5 X 20MM
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321215200·
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311215200·
Life Instruments
FDA UDI
Life Instrument Corporation·M930712152010·Custom 15" Curette #2/0 Ang Light Blue handle
BD INSULIN SYRINGE WITH THE BD ULTRA-FINE¿ NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·March 2, 2018
Life Instruments
FDA UDI
Life Instrument Corporation·M9307121520110·Custom 15" Curette #2/0 Ang Double Bend Light B...
ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EMT-CPAP
FDA 510(k)
FDA Class 2
·Anesthesiology
IH 15° Anatomic Abutment
FDA UDI
SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120484030·
IH 15° Concave Curve Abutment
FDA UDI
SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120483231·
BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·January 13, 2026
BD VACUTAINER® ECLIPSE¿ BLOOD COLLECTION NEEDLE PRE-ATTACHED HOLDER
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·January 13, 2026
ACCU-CHEK ® SPIRIT
FDA Adverse Event
Malfunction
·ROCHE DIABETES CARE AG·Product code LZG·May 21, 2013
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014
ENRHYTHM MRI
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code NVZ·June 13, 2011
BD ULTRA-FINE¿ INSULIN SYRINGE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code FMF·September 14, 2018
EGIA 45 ARTICULATING MED/THICK SULU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·December 9, 2015