BEUDAMED
    65 results · 23ms · Sources: EU EUDAMED, US FDA

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    HERO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434571·Tasso+ convenience kit allows self-collection o...

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528104163·1.6mm Pilot Drill, Long Cannula, Hex

    IMS

    FDA UDI
    HU-FRIEDY MFG. CO., LLC·10889950073312·IMS LG RESIN (16), 1AW, GRY FM

    MicroSelectron Digital

    FDA UDI
    Nucletron B.V.·08717213026087·microSelectron Transfer Tube for 4F Flexibles (19)

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383504096·Gutta Percha Points is used to root canal filin...

    ARDO SUCTION PUMP MASTER, MODEL 30.00.XX; ARDO SUCTION PUMP SENATOR, MODEL 31.00.XX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    AFFIRM DO DIODE LASER

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    UNKNOWN PATHINDER NXT OR INSTINCT JAVA IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code NKB·September 24, 2022

    IMPLANTED GROSHONG PICC

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·May 6, 2013

    DERMABOND ADVANCED TOPICAL SKIN ADHESIVE

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code MPN·September 23, 2014

    SROM STM ST, 30+4L NK, 14X09X130

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code MRA·May 13, 2011

    Helitene Absorbable Collagen Hemostatic Sponge Helitene is indicated in surgical procedures (other than ophthalmological and urological surgery) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

    FDA Enforcement
    Class II ·Terminated·Integra LifeSciences Corporation·May 22, 2013

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code HWC·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 40

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 45

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 35

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019

    TL PEDICLE SCREW DIA. 6,5 LG 50

    FDA Adverse Event
    Malfunction ·ZIMMER SPINE·Product code NKB·July 9, 2019