BEUDAMED
    45 results · 32ms · Sources: EU EUDAMED, US FDA

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    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FILSHIE CLIP (MARK VI) SYSTEM

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FILSHIE CLIP (MARK VI) SYSTEM

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FEMCARE FILSHIE CLIP

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Filshie Clip System

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FEMCARE FILSHIE CLIP

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Filshie Clip (Mark VI) System

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FEMCARE FILSHIE CLIP SYSTEM

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Sterishot II Mini Flishie Clip Applicator

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Filshie Clip (Mark VI) System

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·FILSHIE CLIP(MARK VI) SYSTEM

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Filshie Clip (Mark VI) System

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·Filshie Clip (Mark VI) System

    CC Direct Ti Plastic Cylinder With Hex. W6mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142508·CC Direct Ti Plastic Cylinder With Hex. W6mm

    MODIFIED FERRITIN ENZYME IMUNOASSAY TEST KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    Kit, Assay, Progesterone Receptor

    FDA Pre-Market Approval
    FDA Class 3 ·IMMUNOCYTOCHEMICAL ASSAY TO DETECT PROGESTERONE

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780124665·The humeral trial inserter/extractor is used to...

    MAESTRO FOOT SWITCH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

    MEDTRONIC SURGICAL MECHANICAL VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LWQ·September 11, 2020

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

    Lens, Contact (Other Material) - Daily

    FDA Pre-Market Approval
    FDA Class 2 ·OP-3 (TM) RGP CONTACT LENS