BEUDAMED
    10,000 results · 568ms · 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.

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118395·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118463·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118494·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118487·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118418·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118449·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118364·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118432·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118425·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118357·

    Midmark Extraoral Imaging System (EOIS)

    FDA UDI
    MIDMARK CORPORATION·00841709118500·

    Intraocular Lens

    FDA Pre-Market Approval
    FDA Class 3 ·SENSAR SOFT ACRYLIC UV-LIGHT ABSORBING POSTERIOR CHAMBER INTRAOCULAR LENS

    Inverness Ear Piercing Instruments; Inverness Ear-Nose Piercing Instrument; Inverness Ear Piercing Earring

    FDA registration
    DRL Manufacturing S.A.·1 product·🇩🇴 Dominican Republic

    Automated External Defibrillators (Non-Wearable)

    FDA Pre-Market Approval
    FDA Class 3 ·X Series, Propaq MD, and R Series

    Chambre d’inhalation EG 9 mois - 6 ans

    Device
    EU MDR · Eu Md Class 1 ·Velmedys·On the market·1 country

    Biosynex Chambre d'inhalation 9 mois-6 ans

    Device
    EU MDR · Eu Md Class 1 ·BIOSYNEX·On the market

    PATIENT EXAMINATION GLOVES (LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

    FDA Pre-Market Approval
    FDA Class 3 ·PARADYM CRT-D 8750, PARADYM RF CRT-D 9750 (ZL 102), INTENSIA CRT-D

    Pulse Generator, Permanent, Implantable

    FDA Pre-Market Approval
    FDA Class 3 ·REPLY SR, REPLY DR, ESPRIT SR, ESPRIT DR

    Defibrillator, Implantable, Dual-Chamber

    FDA Pre-Market Approval
    FDA Class 3 ·PARADYM VR 8750, PARADYM DR 8750, PARADYM RF VR 9750, PARADYM RF DR 9750 (ZL102), INTENSIA VR ICD, INTENSIA DR