BEUDAMED
    119 results · 53ms · Sources: EU EUDAMED, US FDA

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    COPAN Diagnostics, Inc.

    FDA registration
    COPAN Diagnostics, Inc.·6 products·🇺🇸 United States

    COPAN DIAGNOSTICS, INC.

    FDA registration
    COPAN DIAGNOSTICS, INC.·14 products·🇺🇸 United States

    TRANSYSTEM¿ / CULTURESWAB¿

    FDA Adverse Event
    Malfunction ·COPAN ITALIA SPA·Product code JSM·July 2, 2024

    FLOQSWAB

    FDA Adverse Event
    Malfunction ·COPAN FLOCK TECHNOLOGIES SRL·Product code KXG·June 12, 2019

    503CS01

    FDA Adverse Event
    Malfunction ·COPAN ITALIA SPA·Product code KXG·August 18, 2020

    FLOCKED SWAB APPLICATOR

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS INCS.·Product code KCJ·December 4, 2009

    FLOQSWABS COPAN FLOCKED SWABS

    FDA Adverse Event
    Injury ·COPAN DIAGNOSTICS INC·Product code KXG·October 21, 2020

    COVID TESTING NASAL SWABS

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code KXG·December 10, 2020

    SWAB

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code KXG·June 26, 2020

    FLOQSWABS

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code KXF·December 17, 2014

    ESWAB

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code JTW·July 19, 2017

    TRANSYSTEM STERILE TRANSPORT SWAB

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code JSM·March 11, 2020

    FLOQSWAB

    FDA Adverse Event
    Malfunction ·COPAN DIAGNOSTICS, INC.·Product code KXG·January 25, 2018

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 27, 2021

    COPAN FLOQSwabs, STERILE.EO, for drawing clinical samples. CE0123, for the following reference numbers REF:501CS01, Minitip, sterile Single Wrapped, Molded bp 80mm; REF: 20226, P/N 501CS01Q100, Minitip, Sterile, Single Wrapped, bp 60MM, BUNDLES OF 20 pcs; REF: 501CS01.Q20, P/N 1127700, Minitip Applicator Sterile Ind. wrapped., bp 60mm, bundles of 20; REF: 502CS01, Regular, Sterile single Wrapped, Molded bp 80mm; REF: 503CS01, Flexible, Sterile Single Wrapped, Molded bp 100mm; REF: 220252, P/N 503CS01.BD, Flexible, Sterile Single Wrapped Molded bp 100 mm; REF: 503CS01/503CS01.BX, Flexible, Sterile Single Wrapped, Molded bp 100mm REF: 50U004DS, hDNA Free, Regular sterile in dry tube Molded Break Point 20 mm; REF: 50U009DS02, hDNA Free, Regular, Sterile, 2pcs Packed; REF: 518CS01, Minitip, Ster. Single Wrapped, Molded bp 100mm; REF: 220251, P/N: 518CS01.BD, Minitip, sterile Single Wrapped Molded bp 100mm; REF: 519C/519C.BX, Regular Sterile, Molded break point 100 mm; REF: 220250 P/N: 519CS01.BD, Regular, Sterile Single wrapped Molded bp 100mm; REF: 525CS01, Ultra-Thin Minitip, sterile single wrapped, molded bp 80 mm; REF: 528C, Large Tip Swab, Handle with Stopper, in dry tube REF: 534CS01, Flexible Nylon, Sterile Single Wrapped; REF: 551C, Minitip Sterile in dry tube, Molded Break Point 80 mm; REF: 552C/552C.BX, Regular sterile in dry tube Molded Break Point 80 mm; REF: 553C, Flexible sterile in dry tube, molded bp 100 mm; REF: 553C.LC, Flexible Sterile in dry tube, molded bp 100 mm; REF: 5U002S, Regular, sterile, in tube, 80 mm breakpoint, with low stopper; 5U048N01.BIO, REF: 5U055S02.HG, Regular FLOQSwabs with 20mm breakpoint 100 peelpouches, 2 swabs per peelpouch; REF: 5U056S.IUO, FLOQSwats ADULT IN DRY TUBE, Investigational Use Only; REF: 5UO57S.IUO, FLOQSwabs CHILD IN DRY TUBE, Investigational Use Only

    FDA Recall
    Terminated ·Copan Italia Via Francesco Perotti 10 Brescia Italy·Product code KXG·July 9, 2021

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·May 7, 2020

    ID NOW COVID 19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·July 1, 2022

    ID NOW COVID-19 TEST KIT 24T (OUS)

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·October 24, 2022

    ID NOW COVID-19 ASSAY

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·September 6, 2022

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·September 22, 2020