BEUDAMED
    28 results · 22ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Open, Classified ×

    Bubble Sensor (REF: 70105.5720)

    FDA Recall
    Open, Classified ·Maquet Medical Systems USA·Product code DTQ·December 28, 2023

    CareFusion V.Mueller GENESIS QTR-LENGTH CONTAINER 12 X 8" (30.3X20.3CM) 4" (10.2CM) DEEP STERRAD COMPATIBLE, REF CD0-4ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD2-4ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD3-6ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS LARGE, SHALLOW CONT. 28 X 11" (71.1 X 27.9CM) 3" (7.6CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-3ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD1-6ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD1-4ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 7" (17.8CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD3-7ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS MINI CONTAINER 10-1/2 X 7-1/2" (26.7X19.0CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD0-3ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 8" (20.3CM) DEEP STERRAD COMPATIBLE, REF CD2-8ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD2-5ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS HALF-LENGTH CONTAINER 11X12" (27.9 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD1-5ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS MID-LENGTH CONTAINER 19X12" (48.3 X 30.5CM) 6" (15.2CM) DEEP STERRAD COMPATIBLE, REF CD2-6ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 5" (12.7CM) DEEP STERRAD COMPATIBLE, REF CD3-5ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS SMALL, SHALLOW CONT. 21 X 7" (53.3 X 17.8CM) 3" (7.6CM) DEEP STERRAD COMPATIBLE, REF CD4-3ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS LARGE, CONTAINER 28 X 11" (71.1 X 27.9CM) 6" (15.2CM) DEEP, PERFORATED STERRAD COMPATIBLE, REF CD5-61ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS FULL-LENGTH CONTAINER 23 X12" (58.4 X 30.5CM) 4" (10CM) DEEP STERRAD COMPATIBLE, REF CD3-4ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    CareFusion V.Mueller GENESIS SMALL CONTAINER 21 X 7" (53.3 X 17.8CM) 5-1/2" (14CM) DEEP STERRAD COMPATIBLE, REF CD4-5ST

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code KCT·September 26, 2022

    PCA 4000 Curing Units, SKU number ACC-06-1000 The PCA 4000 is used for curing industrial resins as well and this recall will not impact units sold to industrial customers.

    FDA Recall
    Open, Classified ·Envisiontec US Llc·Product code EBZ·January 20, 2022

    (1) CryoPatch SG Pulmonary Human Cardiac Hemi-Artery - Artery Patch, SGPH00 Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology; and (2) CryoPatch SG Pulmonary Human Cardiac Branch Patch, SGP020, Cryopreserved Decellularized Cardiac Tissue Allograft Prepared with SynerGraft (SG) Technology.

    FDA Recall
    Open, Classified ·Artivion, Inc·Product code DXZ·May 28, 2024