BEUDAMED
    21 results · 19ms · 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.

    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·RESONEX RX4000{TM} MAGNETIC RESONANCE IMAGING SYST

    System, Nuclear Magnetic Resonance Imaging

    FDA Pre-Market Approval
    FDA Class 2 ·RESONEX RX4000{TM} MAGNETIC RESONANCE IMAGING SYST

    OCULAB PACHPEN

    FDA 510(k)
    FDA Class 2 ·Radiology

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·PARAPERM O2 CLEAR & BLUE LENS

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    Laser, Neodymium:Yag, Ophthalmic For Uses Other Than Posterior Capsulotomy & Cutting Pupillary

    FDA Pre-Market Approval
    FDA Class 3 ·ND:YAG POSTERIOR CAPSULOTOMY MODEL 100

    CRYSTALLINE PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·June 10, 2014

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·October 31, 2012

    BD PLASTIPAK SYRINGE WITH NEEDLE 26G X 3/8"

    FDA Adverse Event
    Injury ·BD·Product code FMF·June 16, 2015

    IQon Spectral CT with 4.7.2 software version.- Model 728332, a Philips Computed Tomography X-Ray System

    FDA Enforcement
    Class II ·Terminated·Philips Medical Systems (Cleveland) Inc·March 14, 2018