BEUDAMED
    35 results · 31ms · Sources: EU EUDAMED, US FDA

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    KENDALL 14.5 FR MAXID CUFFED DUAL LUMEN CATHETER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LOCATOR R-Tx

    FDA UDI
    Zest Anchors, LLC·00840481126062·LOCATOR R-Tx Limited Range Retention Inserts, H...

    LOCATOR, Dentsply Sirona System

    FDA UDI
    Zest Anchors, LLC·00840481131820·LOCATOR R-Tx Limited Range Retention Inserts, H...

    LOCATOR F-Tx

    FDA UDI
    Zest Anchors, LLC·00840481114380·LOCATOR F-Tx Attachment System, Latch Driver

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993135806·CUSTOM SEAMLESS SOFT 3/KNEE HIGH/CLOSED TOE/DOT...

    JOBST Custom Seamless Soft

    FDA UDI
    BSN-Jobst GmbH·04059993129928·CUSTOM SEAMLESS SOFT 1/KNEE HIGH/CLOSED TOE/DOT...

    Diamondback Peripheral

    FDA UDI
    Cardiovascular Systems, Inc.·10852528005350·Diamondback Peripheral, Radial Access OAD, 1.25...

    Compumedics Quik-Cap

    FDA UDI
    COMPUMEDICS LIMITED·09342451004635·Quik-Cap Neoprene Flexnet - Grael 64 Ch Small

    Compumedics Neuvo

    FDA UDI
    COMPUMEDICS LIMITED·09342451001146·Bracket - System Unit Neuvo System Mounting Kits

    KLINIDRAPE SURGICAL GOWNS, NON-REINFORCED, BASIC PROTECTIONS AND STANDARD PROTECTION

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

    POLY PER-Q-CATH PICC CATHETER,MODEL 3236100 AND POLY PER-Q-CATH MIDLINE CATHETER, MODEL 3134135

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 13, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 15, 2006

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54, 55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURGERY REUSABLE DEVICES, HANDPIECE 54,55

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006