23 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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LIVE VIEW PANEL (LVP)
FDA 510(k)
FDA Class 2
·Neurology
Gyrus ACMI
FDA UDI
Gyrus ACMI, LLC·00821925018624·LID FOR LARGE STERILIZATION TRAY
DD tempMED
FDA UDI
Dental Direkt GmbH·EDDIK114151·DD tempMED are pre-colored dental milling blank...
ArgenIS
FDA UDI
ARGEN CORPORATION, THE·D818131415·TiBase DX RP.3G NE
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981215132·Interbody, 39mm x 30mm x 14mm, 15 Deg
3D Printed Interbody System
FDA UDI
Seaspine Orthopedics Corporation·10889981303648·Interbody, 39mm x 30mm x 14mm, 15 Deg, 3D
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981217037·Trial, 39mm x 30mm x 14mm, 15 Deg
BD PLASTIPAK¿ STERILE PLASTIC SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON DE MEXICO·Product code FMF·February 2, 2022
SPII Model Lubinus Hip Stem - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575385782·Surgical implant template, reusable - SPII Mode...
SPII Model Lubinus Hip Stem - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575385768·Surgical implant template, reusable - SPII Mode...
SPII Model Lubinus Hip Stem - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575385775·Surgical implant template, reusable - SPII Mode...
MOLLRING MULTITASC
FDA 510(k)
FDA Class 2
·Cardiovascular
THERACLEAR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CART 9733856 S7 STAFF ASSEMBLED 110V
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019
STEALTHSTATION® S7´
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 20, 2019
CART 9733856 S7 STAFF ASSEMBLED 110V
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 17, 2019
SURESCAN
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 1, 2014
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DTE·June 16, 2011
HUDSON ET TUBE, SHER-I-BRONCH, LS, 39 FR
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTR·October 7, 2015
MITRACLIP G4 CLIP DELIVERY SYSTEM (MDD)
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NKM·March 5, 2024