BEUDAMED
    52 results · 21ms · 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 Regulation: Us FDA ×

    PEAK PULSAR II GENERATOR MODEL PS100-102

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

    Synergy

    FDA UDI
    Rmo, Inc.·00885797375872·COLUMBIA SYN ROTH 022 HK2345

    SPIRA-C

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPC1020290·Trial, 16mm x 20mm Lordotic 7°, 9mm

    SPIRA-L

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPL1020290·Trial, Bi-Convex, 8° Lordotic, 26 x 60mm, 14mm

    SPIRA-A

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPA1020290·Trial, 30 x 38mm, 8° Lordotic, 19mm

    SPIRA-O

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SPO1020290·Trial Bi-Convex 15° Lordotic, 30mm x 33mm, 17mm

    SPIRA®-A Integrated

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1020290·SPIRA®-A Integrated,Trial, 26x34mm, 8° Lordotic...

    REMEDY MODEL 2Z12

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ZOLL M SERIES NIBP OPTION, MODEL MSERIES NIBP OPTION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711020290130·Lateral Midfoot Charcot Guide, 29mm x 13mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711020290110·Lateral Midfoot Charcot Guide, 29mm x 11mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711020290120·Lateral Midfoot Charcot Guide, 29mm x 12mm

    Intelliguides

    FDA UDI
    Mios Marketing, LLC·G2711020290100·Lateral Midfoot Charcot Guide, 29mm x 10mm

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970010·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172970027·

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172974018·UniTip High Resolution Catheter 10F

    ADAPTER 040F, STERILE

    FDA Adverse Event
    Malfunction ·MEDLINE INDUSTRIES, LP·Product code BTT·April 24, 2026

    DOUBLE MOBILITY LINER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·April 3, 2025

    ECOFLX 500 ML EMPTYING MIXTURE BAG

    FDA Adverse Event
    Malfunction ·DOUGLAS MEDICAL PRODUCTS, INC.·Product code KPE·August 11, 2025

    MOTO PARTIAL KNEE SYSTEM - MEDIAL

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code HSX·August 12, 2025