BEUDAMED
    260 results · 22ms · Sources: EU EUDAMED, US FDA

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    Halyard Lavender, Low Dermatitis Potential, Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs and and Fentanyl Citrate

    FDA 510(k)
    FDA Class 1 ·General Hospital

    NA

    FDA UDI
    Synthes GmbH·10886982144331·3.0MM CANNULATED SCREW SHORT THREAD/22MM

    36M - MSHA Miners

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588026206·36M - MSHA Miners

    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113325·PHACO KNIFE 2.8MM ANGLED (BX/5)

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383513401·"An absorbent paper points is an endodontic pap...

    Medical Facets NC

    FDA UDI
    MEDICAL FACETS NC LLC·M933MDF2026220·3.0mm Cannulated Screw, Short Thread, 22mm

    Diamond Orthopedic, LLC

    FDA UDI
    DIAMOND ORTHOPEDIC, LLC·B551DMD2026220·3.0mm, Cannulated Screw, Short Thd., 22mm

    CEM-OSTETIC, MODELS CEMO-020O, CEMO-05P, CEMO-10P, CEMO-20P, AND CEMO-30P

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOSLEEP

    FDA 510(k)
    FDA Class 2 ·Neurology

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·March 23, 2026

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 22, 2025

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 17, 2026

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 10, 2026

    MINIMED 780G US SYSTEM BLE CONNECT 3.0 MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 27, 2026

    PUMP 1886 780G OUS BLE PUMP MG/DL

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·February 2, 2026

    GMK SPHERE TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 14, 2026

    OPTIFLUX 160NRE DIALYZER FINISHED ASSY.

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA, OGDEN MANUFACTURING·Product code FJI·September 18, 2014

    SYMPHONY

    FDA Adverse Event
    Injury ·SORIN CRM·Product code NVZ·August 8, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·July 2, 2013

    GMK-SPHERE TIBIAL TRAY FIXED CEMENTED SIZE 2 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·July 3, 2024