BEUDAMED
    114 results · 18ms · Sources: EU EUDAMED, US FDA

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    Glucose reagent

    FDA UDI
    M DIALYSIS INC.·07332699000652·

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE/CONDYLAR PROSTHESES

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE/CONDYLAR PROSTHESIS SYSTEM AND TMJ FOSSA-EMINENCE PROSTHESIS

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE AND CONDYLAR PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE AND CONDY LAR PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·FOSSA-EMINENCE & CONDYLAR PROSTHESIS SYSTEM AND FOSSA-EMINENCE PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·FOSSA-EMINENCE & CONDYLAR PROSTHESIS SYSTEM AND FOSSA-EMINENCE PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA EMINENCE PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE AND CONDYLAR PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE & CONDYLAR PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE AND CONDYLAR PROSTHESIS SYSTEM

    Joint, Temporomandibular, Implant

    FDA Pre-Market Approval
    FDA Class 3 ·TMJ FOSSA-EMINENCE AND CONDYLAR PROSTHESIS SYSTEM

    SABLE Rotamax PRO 45KL

    FDA UDI
    Sable Industries Inc·00841359010056·SABLE Rotamax PRO 45KL is a 45 degree Push Butt...

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950023585·RONGEUR #5 CLEVELAND 6-3/4" 17CM

    N/A

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994989697·RONGEUR 2000023

    LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023

    FDA Recall
    Open, Classified ·Physio-Control, Inc.·Product code MKJ·September 29, 2023

    LIFEPAK 15, REF: 99577-001958, Part Number: V15-7-000023

    FDA Enforcement
    Class II ·Ongoing·Physio-Control, Inc.·November 22, 2023

    General Instrument

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132124925·Flex Nail Bender

    AP423- MICROBORE WITH NON-VENTED SPIKE AND A BACK CHECK VALVE

    FDA UDI
    EITAN MEDICAL LTD·17290109159239·

    AP423-01 MICROBORE WITH VENTED NON-VENTED SPIKE AND A BACK CHECK VALVE

    FDA UDI
    EITAN MEDICAL LTD·17290109154630·