41 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Tigereye CTO-Crossing Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
Accufit
FDA UDI
Ortho Organizers, Inc.·00190707183813·Accufit Molar Bands Lower Right First Molar 33
NA
FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252634393·PED. MAND. DISTRACTOR, 2x2 LEFT, 30 MM
Life Instruments
FDA UDI
Life Instrument Corporation·M93072013300F0·Flat Cobb Elevator 30mm 7" handle
Life Instruments
FDA UDI
Life Instrument Corporation·M930720133000·Long Cobb Elevator 30mm 7" handle
Symmetry Olsen
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00841785103728·
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383511186·"An absorbent paper points is an endodontic pap...
Viceroy
FDA UDI
DIOMEDICAL CO.,LTD.·08800113905245·VICEROY Rod - 6.0 (D)6x(L)330mm
SOVEREIGN BIPOLAR INSTRUMENTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MAGNETOM TRIO QUADRATURE TX/RX HEAD COIL
FDA 510(k)
FDA Class 2
·Radiology
BECKER TEAR DROP
FDA UDI
The Wells Johnson Company·B458201330000·Cannula, Becker Tear Drop, specify length, diam...
DANmed
FDA UDI
DANNORITZER Medizintechnik GmbH & Co. KG·04251351101236·LAP- Electrode, monop., Ø5mm, l=330mm
"J" - ...
BIPOLAR MACRO FORCEPS D:5/ 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·April 6, 2015
ARCHITECT TACROLIMUS
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code MLM·January 28, 2013
BIPOLAR MARYLAND DISS.FCPS 5MM 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO KG·Product code GEI·March 9, 2015
JAW INS.BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014
JAW INS. BIP.MARYLAND DISS.FEN.5/310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM, DEXCOM SHARE SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·December 14, 2015
MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 23, 2017