BEUDAMED
    104 results · 21ms · Sources: EU EUDAMED, US FDA

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    ATTAIN PREVAIL STEERABLE CATHETER SET, MODEL 6228CTH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Audit MicroControls Control FD Assayed Chemistry, Level 2

    FDA UDI
    AALTO SCIENTIFIC·B085K0312100·

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0132110·Trial, TLIF, 27L OB CRV 7Deg, 11mm

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K0112110·Tap, Cannulated, 4.75 mm

    FLOWABLE COMPOSITE/ ECUFLOW/ LUXAFLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO INTRALASE 600C LASER KERATOME

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

    INTACS PRESCRIPTION INSERTS

    FDA Adverse Event
    Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·April 2, 2013

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code MDS·March 16, 2011

    PUMP MMT-722NAL PRDGM INS V2.2 CL EN PR

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·April 17, 2008

    MONOPLUS VIOLET 0 (3,5) 90CM HR37S(M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.U.·Product code NEW·December 14, 2021

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 2, 2019

    MONOPLUS VIOLET 4/0 (1.5) 70CM HR17 (M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 23, 2019

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·June 2, 2022

    MONOPLUS VIOLET 3/0 (2) 70CM HR22 (M)RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·July 30, 2021

    MONOMEND MAX 2/0 (3)70CM HS37S(M)VPL DDP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·August 13, 2021

    MONOPLUS VIOLET 4/0(1,5)4X45 HR22 TO(M)

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·October 2, 2019

    MONOMEND MAX 3/0 (2) 70CM DS24(M)VPL RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·July 31, 2023

    MONOPLUS C VIOLET 2/0 (3) 25M

    FDA Adverse Event
    Malfunction ·B.BRAUN SURGICAL SA·Product code NEW·January 30, 2019

    MONOMEND MAX 2/0 27" (70CM)HR26S VPL RCP

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL, S.A.·Product code NEW·November 7, 2022