BEUDAMED
    11 results · 14ms · Sources: EU EUDAMED, US FDA

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    STEALTH SPRING CLIP 6mm latis (3/4 Force). REF/UDI::A1603/(01)00607915110581 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

    FDA Recall
    Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code DSS·January 31, 2020

    STEALTH SPRING CLIP 6mm latis (1/4 Force). Non-Sterile, REF/UDI::A1702/(01)10607915110649 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

    FDA Recall
    Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code DSS·January 31, 2020

    Contact Nipple Shield (Sterile) - 24mm (Standard); Individually wrapped silicone contact nipple shields for immediate use for latch-on difficulties while breastfeeding the baby under professional care only; Manufactured for Medela, Inc., P.O. Box 660, McHenry, IL 60051-0660, Made in Switzerland; article #67203S Individually wrapped for immediate use. For latch-on difficulties. Made of silicone. For use under professional care only while breastfeeding the baby.

    FDA Recall
    Terminated ·Medela Inc·Product code HFS·May 18, 2011

    STEALTH SPRING CLIP 6mm latis (1/2 Force). REF/UDI::A1601/(01)00607915110567 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

    FDA Recall
    Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code DSS·January 31, 2020

    STEALTH SPRING CLIP 6mm latis (1/4 Force). REF/UDI::A1602/(01)00607915110574 - Product Usage: The device is indicated for surgical clamping during cardiovascular, peripheral vascular, and general surgery.

    FDA Recall
    Terminated ·Applied Medical Resources Corp 22872 Avenida Empresa Rancho Santa·Product code DSS·January 31, 2020

    SSCOR Suction Device Model 2310V

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2310BV

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2310BV-230

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2315

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2314

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005

    SSCOR Suction Device Model 2314B

    FDA Recall
    Terminated ·S S C O R Inc·Product code BTA·January 6, 2005