BEUDAMED
    29 results · 24ms · Sources: EU EUDAMED, US FDA

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    ECHO TIP ULTRA FIDUCIAL NEEDLE

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

    Regenerex

    FDA UDI
    Biomet Orthopedics, LLC·00880304554412·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515065895·Roch-Ochs Hemo Fcps, str, 1x2 tth, 8 3/4"

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515018754·Roch-Ochs Hemo Fcps, str, 1x2 tth, 8 3/4"

    RGX 3 PEG SER A PATELLA

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code HRY·July 1, 2019

    ARTHREX TENODESIS SCREW FAMILY

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Spacer-G and Spacer-K

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CERVICAL PLATE VARIABLE SELF-TAPPING SCREW DIAM. 4X14MM (2X)

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KWQ·June 8, 2018

    E1 VNGD PS+ TIB BRG 71/75X10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OIY·December 8, 2020

    REGENEREX BIOMENT PRIMARY TIBIAL TRAY WITH LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 21, 2017

    VANGUARD CR FEMORAL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 21, 2017

    VANGUARD TIBIAL BEARING CR LIPPED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·December 21, 2017

    UNIDENTIFIED CORAIL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code KWA·June 3, 2013

    KARL STORZ

    FDA Adverse Event
    Other ·KARL STORZ GMBH & CO. KG·Product code FBP·June 14, 2011

    BAG 4X6 10M 225ML VOL, MONARCH RETRIEVAL BAG

    FDA Adverse Event
    Other ·APPLIED MEDICAL RESOURCES·Product code GCJ·August 28, 2008

    VANGUARD POSTERIOR STABILIZED E1 ANTIOXIDANT INFUSED TIBIAL BEARING 14MM X 71/75

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 23, 2019

    VANGUARD POSTERIOR STABILIZED OPEN BOX FEMORAL COMPONENT LEFT 65MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 23, 2019

    REGENEREX PRIMARY TIBIAL TRAY WITH LOCKING BAR 71MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 23, 2019

    BIOMET MODULAR FINNED STEM WITH SCREW 80MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·July 23, 2019

    Knee Products: 141356 Regenerex Series-A Patella 3 Peg, 31 MM 141358 Regenerex Series-A Patella 3 Peg, 37 MM Product Usage: Knee prosthesis

    FDA Recall
    Terminated ·Biomet, Inc.·Product code MBH·April 17, 2020