BEUDAMED
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    CRIT-LINE CLIP (CLIC) BLOOD CHAMBER

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

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515065680·Rankin Fcps, cvd, 6 1/4"

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515018273·Rankin Fcps, cvd, 6 1/4"

    VEGA KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DATASCOPE 7.5FR. IAB CATHETER AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AS VEGA PS TIBIAL PLATEAU CEMENTED T3

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 4, 2018

    LINEAR 7.5 FR. 25CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

    LINEAR 7.5 FR. 25CC IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·October 17, 2019

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 3, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 3, 2013

    ASR ACETABULAR CUPS 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011

    AS COLUMBUS REV F FEMUR CEMENTED F5L

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS VEGA PS TIBIAL PLATEAU CEMENTED T3+

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS VEGA PS TIBIAL PLATEAU CEMENTED T2

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS COLUMBUS REV F TIB.OFFSET CEMENT.T5

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    2.7MM/3.5MM TI LCP LAT DISTAL FIBULA PLATE 7H/LEFT/125MM

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·November 12, 2018

    LINEAR 7.5 FR. 40CC IAB

    FDA Adverse Event
    Injury ·DATASCOPE CORP. - FAIRFIELD·Product code DSP·May 14, 2020

    AS VEGA PS FEMORAL COMP.CEMENTED F5N R

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code JWH·March 23, 2018

    AS VEGA PS FEMORAL COMP.CEMENTED F4N R

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS·Product code JWH·March 23, 2018

    AS VEGA PS FEMORAL COMP.CEMENTED F6N R

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018