BEUDAMED
    27 results · 19ms · Sources: EU EUDAMED, US FDA

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    S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CTXA Hip Bone Mineral Densitometer

    FDA UDI
    MINDWAYS SOFTWARE, INC.·B052DICTXAHIP0·The CTXA Hip Bone Mineral Densitometer (CTXA Hi...

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002116·artVeneer life upper posteriors, S, C3

    BetaForce™

    FDA UDI
    Ortho Organizers, Inc.·00190707124458·BETAFORCE Beta³ Euro Upper 16x16 (10pk)

    BetaForce

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730022042·Beta3 Euro Upper 16x16 10 archwires per pack

    BetaForce

    FDA UDI
    ORTHO TECHNOLOGY, INC.·00190730020161·Beta Titanium U/L 16x25 10 archwires per pack

    BetaForce™

    FDA UDI
    Ortho Organizers, Inc.·00190707124311·Beta Titanium U/L 16x25 (10pk)

    SCANLAN®

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159007848·Hunter-Satinsky Aorta Clamp

    Metal Custom Rx

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746102400·BRACKET MEDIUM TWIN 022 TQ=25 A=0 R=0 PROFILE=S...

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981212810·Trial 11w, 16mm

    POWDER-FREE LATEX EXAMINATION GLOVE STERILE WITH OPTIONAL PROTEIN LABELING CLAIM (50 MICROGRAMS OR LESS)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    QUALITROL URINALYSIS WITH MICROSCOPICS CONTROL, LEVELS 1,2 AND 3

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    NA

    FDA UDI
    STRYKER CORPORATION·04546540030375·1.7mm Steiger Carbide Bur

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150977·Angled Cup Curette Size 4

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523150694·Solid 3.5mm Hex Driver, Long Shaft

    ASSERT-IQ¿ ICM

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code MXC·October 7, 2025

    CRONIN SILASTIC IMPLANT

    FDA Adverse Event
    DOW CORNING CORP.·Product code FTR·May 19, 1994

    HEYER-SCHULTE BREAST IMPLANT, 165 CC

    FDA Adverse Event
    V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·May 19, 1994

    MINMED QUICK SET

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 8, 2024

    HEARTSINE SAMARITAN 300P AND PAD PAK

    FDA Adverse Event
    Malfunction ·HEARTSINE TECHNOLOGIES, LTD·Product code MKJ·February 11, 2013