440 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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REGIUS SIGMA2
FDA 510(k)
FDA Class 2
·Radiology
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780376996·Integra® Jarit® Crile-Wood Needle Holder, 7-1/4"
Hayden Medical
FDA UDI
Hayden Medical, Inc.·00840319739495·Adson Tissue Forceps 4-3/4" (11.9cm), 1x2 teeth...
PMT® CORPORATION HALO
FDA UDI
PMT CORPORATION·00650551044826·COMBINATION WRENCH OPEN END/BOX WRENCH
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·10884450259532·
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131101·IN-OVATION® C Base Rx 018 U3-3 CS HK
IN-OVATION® C
FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K100131611·IN-OVATION® C Roncone 018 U3-3 CS HK
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197030762·Fomon lower lateral scissors
115mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197030779·Fomon dissecting scissors
135mm,...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197030755·Fomon Lower Lateral Nasal Scissors
strong...
NANO-CHECK AMI CTNI CARDIAC MARKER TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
VENUS UNIVERSAL LIGHT CURING COMPOSITE
FDA 510(k)
FDA Class 2
·Dental
Widex
FDA UDI
Widex A/S·05706069920352·WIDEX MOMENT MBB3D 330 DEMO (Silver grey)
ASR XL TAP SLV ADAP 12/14+2
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 20, 2013
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·September 25, 2014
PRECISE PAIN RELIEVING HEAT PATCH
FDA Adverse Event
Injury
·KIRIBAI KOBAYASHI PHARMACEUTICAL CO, LTD·Product code IMD·June 3, 2011
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 17, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·September 19, 2025
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code NJR·April 17, 2026
BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·May 20, 2026