BEUDAMED
    24 results · 31ms · Sources: EU EUDAMED, US FDA

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    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·HULKA CLIP FOR TUBAL OCCLUSION

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·HULKA CLIP FOR TUBAL OCCLUSION

    Laparoscopic Contraceptive Tubal Occlusion Device

    FDA Pre-Market Approval
    FDA Class 3 ·HULKA CLIP FOR TUBAL OCCLUSION

    Pilling

    FDA UDI
    Avalign Technologies, Inc.·00190776143633·Esophageal Retractor, Flushable Port

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556700775·GC Initial™ MC Clear Window CL-W, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228700801·GC Initial™ MC Clear Window CL-W, 20g

    8.7 mm X 80 mm iFuse TORQ TNT Implant

    FDA UDI
    Si-Bone Inc.·00810055524242·8.7 mm X 80 mm iFuse TORQ TNT Implant

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

    FDA Pre-Market Approval
    FDA Class 3 ·PICOLAS NEODYMIUN-YAG OPHTHALMIC LASEER

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019517078008·

    Portex

    FDA UDI
    ICU MEDICAL, INC.·15019315038808·

    MICRO-EAR FULL-CONCHA IN-THE-EAR HEARING AID

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·SEREINE CLEANER

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·SEREINE CONTACT LENS CLEANER (NEW PRESERVATIVE)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·SEREINE CONTACT LENS CLEANER (NEW PRESERVATIVE)

    Accessories, Soft Lens Products

    FDA Pre-Market Approval
    FDA Class 2 ·SEREINE CLEANER,15ML NEW SAMPLE SIZE

    PORTEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·August 7, 2020

    PORTEX BLUE LINE ULTRA SUCTIONAID TUBE WITH SOFT-SEAL CUFF AND INNER CANNULAE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·June 26, 2019

    PORTEX BLUE LINE ULTRA SUCTIONAID TUBE WITH SOFT-SEAL CUFF AND INNER CANNULAE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JOH·June 26, 2019

    PORTEX

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·August 29, 2020

    BLUE LINE ULTRA

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC·Product code JOH·July 18, 2019