29 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Electronic Sphygmomanometer (Model: LT-P30)
FDA 510(k)
FDA Class 2
·Cardiovascular
BD™ Universal Viral Transport for Viral, Specimens
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902202203·Vial Universal Viral Transport
BD Universal Viral Transport
FDA UDI
COPAN ITALIA SPA·38053326009335·3 mL Vial
InstaTemp® Max Temp. Material Mixing tips 45 pcs.
FDA UDI
STERNGOLD DENTAL LLC·00841549115981·Mixing tips used for dispensing material from a...
APEX PS Knee
FDA UDI
Omni Life Science, Inc.·00841690113133·PS Insert, Size 2 x 20mm
Coral
FDA UDI
Seaspine Orthopedics Corporation·10889981029234·Fixed X-Conn 20mm
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197312813·TC Gorney Septum Morselizer
angled...
BD¿ UNIVERSAL VIRAL TRANSPORT KIT, 3 ML VIAL
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSM·July 29, 2022
ADAPTAIN SOLUBLE IMPLANT MATERIAL
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
ULTRASONIC STRAIGHT/ULTRASONIC KNIFE/ULTRASONIC RING CURRETTE
FDA 510(k)
FDA Unclassified
·Unknown
UNK_SMART TOUCH UNIDIRECTIONAL SF
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·June 22, 2023
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code ITI·November 3, 2014
INTERSTIM II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 16, 2011
DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·July 11, 2013
MENTOR SMOOTH ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·May 28, 2020
MENTOR SMOOTH ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·May 28, 2020
ConMed System 2450 Electrosurgical Generator, REF 60-2450-220, 220 V, ConMed Electrosurgery, Centennial, CO. A general-purpose electrosurgical generator used in conjunction with an electrosurgical accessory handpiece for delivery of high (HF) electrosurgical current through an accessory electrode for cutting and coagulation at the operative site.
FDA Recall
Terminated
·ConMed Electrosurgery·Product code GEI·December 27, 2010
COBAS SARS-COV-2 & INFLUENZA A/B FOR USE ON THE COBAS 6800-8800 SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·May 13, 2021
COBAS SARS-COV-2 & INFLUENZA A/B TEST FOR USE ON THE COBAS LIAT SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·June 21, 2021
COBAS SARS-COV-2 & INFLUENZA A/B FOR USE ON THE COBAS 6800-8800 SYSTEM
FDA Adverse Event
Malfunction
·ROCHE MOLECULAR SYSTEMS, INC. - BRANCHBURG·Product code QJR·May 13, 2021