BEUDAMED
    32 results · 13ms · Sources: EU EUDAMED, US FDA

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    RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product Usage: Tracheal intubation during laser surgery in the laryngeal area. The tube is resistant to the following kinds of laser: A R+ laser / ND/YAG laser / CO2 lasers (continuous-wave or pulsed) with a wave length ranging from 0.488 m to 10.6 m.

    FDA Recall
    Terminated ·TELEFLEX MEDICAL INC·Product code BTR·May 29, 2020

    Restoration Hip system Cylindrical Distal Extension. Catalog Numbers 1212-3105, 1212-3115, 1212-3125, and 1212-3195. Sizes 12.5mm, 11.5mm, 19.5mm, and 10.5mm extensions.

    FDA Recall
    Terminated ·Stryker Howmedica Osteonics·Product code LXH·February 10, 2004

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·April 1, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·April 1, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·April 1, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·April 1, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0

    FDA Recall
    Terminated ·Teleflex Medical·Product code BTR·April 1, 2019

    Symmetric Total Knee Femoral Components Product Usage: Symmetric Total Knee Femoral Component is intended for use with Signal Medical Corp. Total Knee System for cemented use INA Total Knee Replacement. The femoral component is made of cobalt chromium alloy (ASTM F75).

    FDA Enforcement
    Class II ·Terminated·Signal Medical Corporation·October 29, 2014

    RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product Usage: Tracheal intubation during laser surgery in the laryngeal area. The tube is resistant to the following kinds of laser: A R+ laser / ND/YAG laser / CO2 lasers (continuous-wave or pulsed) with a wave length ranging from 0.488 ¿m to 10.6 ¿m.

    FDA Enforcement
    Class II ·Terminated·TELEFLEX MEDICAL INC·July 15, 2020

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000080, REF 102004, SIZE I.D. mm 8,0

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·June 5, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000050, REF 102004, SIZE I.D. mm 5,0

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·June 5, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·June 5, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000060, REF 102004, SIZE I.D. mm 6,0

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·June 5, 2019

    RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

    FDA Enforcement
    Class II ·Terminated·Teleflex Medical·June 5, 2019

    Radionics Head and Neck Localilizer (HNL), Version B

    FDA Recall
    Terminated ·Radionics, Inc.·Product code MUJ·May 25, 2004

    Alsius CoolGard 3000 patient temperature regulation system

    FDA Recall
    Terminated ·Alsius Corporation·Product code NCX·November 10, 2004

    Biolox Ceramic Head XL

    FDA Recall
    Terminated ·Plus Orthopedics·Product code LZO·February 10, 2004

    Optima Spinal System and Spinal Hook System, set screw component.

    FDA Recall
    Terminated ·U & I America·Product code MNI·August 10, 2004

    VerifyNow Asprin Assay Kit Part No. 85034

    FDA Recall
    Terminated ·Accumetrics Inc·Product code JOZ·May 10, 2004

    Foundation Knee System, Tibia-Nonporous, Size 6, Right, sterile. Manufactured by Encore Orthopeadics, 9800 Metric Blvd., Austin, Texas 78758

    FDA Recall
    Terminated ·Product code JWH·May 10, 2004