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

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    RIVA SC

    FDA UDI
    SDI LIMITED·09336472015572·RIVA SC A3.5 REG 50 CAP

    RIVA SC

    FDA UDI
    SDI LIMITED·DO3686000041·

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR86000041·Max. 1.+2. Bicuspidband 04

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169774·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 6...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169811·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 1...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169798·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 8...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169781·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 7...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169767·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 5...

    Arsenal

    FDA UDI
    ALPHATEC SPINE, INC.·00840967169804·EXTENDED BODY NARROW BLADE INFRALAMINAR HOOK, 9...

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR86000040501·Max. 1.+2. Bicuspidband 04

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR86000040101·Max. 1.+2. Bicuspidband 04

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR86000040051·Max. 1.+2. Bicuspidband 04

    BL, Ø 4.8MM RC, SLA® 8MM, TI, LOXIM

    FDA Adverse Event
    Injury ·INSTITUT STRAUMANN AG·Product code DZE·January 29, 2024

    OMNISPAN MENISCAL REPAIR 27DEG

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·May 10, 2019

    The Model 8540 Catheter Access Port Kit is intended for use in accessing the catheter via the catheter access port of Medtronic(R) implantable programmable infusion pumps (except Medtronic MiniMed pumps). The Model 8540 Catheter Access Port Kit does not have a product code for itself; it is approved under PMA P860004. PMA P860004 is classified as: pump, infusion, implanted, programmable under product code LKK.

    FDA Recall
    Terminated ·Medtronic Inc, Neurological & Spinal Division·Product code LKK·July 23, 2004

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 29, 2016

    IMPLANTABLE DRUG INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·November 7, 2024

    Model 8561 Lioresal (Baclofen injection) Intrathecal Refill Kit is designed for refilling the Medtronic SynchroMed family of pumps. The 8561 kit contains a 1-20 ml ampule of 500 mcg/ml Baclofen injection along with a sterile refill kit tray and sterile drug preparation tray. Lioresal drug ampules contained witin Medtronic Lot N0016487 bear the primary manufacturer''s label and lot number 007J2583. The drug box is labeled with Lot 017H1925. Medtronic packages a manufacturer''s labeled ampule into a protective drug box. A lot number and drug lot expiration date are printed on the outside of the drug box. The filled and labeled drug box is placed inside a larger kit assembly that contains other components necessary to complete a pump refill. Only the large kit assembly (''Lioresal Refill Kit'') will display the Medtronic lot number (N0016487). The Model 8561 refill kit does not have a product code for itself; it is approved under PMA P860004. PMA P860004 is classified as: pump infusion, implanted, programmable under product code LKK.

    FDA Recall
    Terminated ·Medtronic Inc, Neurological & Spinal Division·Product code LKK·November 19, 2004

    Pump, Infusion, Implanted, Programmable

    FDA Pre-Market Approval
    FDA Class 3 ·MEDTRONIC(R) SYNCHROMED(TM) PUMP & INFUSION SYSTEM

    Pump, Infusion, Implanted, Programmable

    FDA Pre-Market Approval
    FDA Class 3 ·SynchroMed Infusion System, Intrathecal Catheters