BEUDAMED
    3,081 results · 48ms · Sources: EU EUDAMED, US FDA

    TS-1 TS-2

    Basic UDI-DI
    EU MDR · Eu Md Class 2a ·Jiangsu Zhengkang Medical Apparatus Co.,Ltd.·2 devices

    811-B; 811-BL; 811-BTS; 842; 909; 841-A; 801-B; 812; 840; 915-BL; 806-CB; 810-A; 810-B

    FDA registration
    PARKS MEDICAL ELECTRONICS, INC.·1 product·🇺🇸 United States

    easy ray patient positioning

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MTS Maschinenbau AG·2 devices

    easy ray X-ray table

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MTS Maschinenbau AG·1 device

    easy ray Trägereinheit

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MTS Maschinenbau AG·12 devices

    easy ray Schwenkbügelstativ

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·MTS Maschinenbau AG·6 devices

    QuikCoag Control Level 3 High Abnormal

    FDA UDI
    Biomedica Diagnostics Inc·00627944000080·

    QuikCoag Control Level 1 Normal

    FDA UDI
    Biomedica Diagnostics Inc·00627944000066·

    CRYOcheck™ Abnormal 1 Control

    FDA UDI
    Precision Biologic Inc·00843876000107·

    QuikCoag Control Level 2 Low Abnormal

    FDA UDI
    Biomedica Diagnostics Inc·00627944000073·

    CRYOcheck™ Abnormal 2 Control

    FDA UDI
    Precision Biologic Inc·00843876000114·

    Filler, Bone Void, Synthetic Peptide

    FDA Pre-Market Approval
    FDA Class 3 ·i-FACTOR Peptide Enhanced Bone Graft

    Coronary Drug-Eluting Stent

    FDA Pre-Market Approval
    FDA Class 3 ·SYNERGY XD Everolimus Eluting Platinum Chromium Coronary Stent System and SYNERGY SHIELD Everolimus Eluting Platinum Chr

    Implant, Dermal, For Aesthetic Use

    FDA Pre-Market Approval
    FDA Class 3 ·SCULPTRA AESTHETIC (INJECTABLE POLY-L-LACTIC ACID)

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·Zenith Dissection Endovascular System

    Lens, Intraocular, Phakic

    FDA Pre-Market Approval
    FDA Class 3 ·STAAR SURGICAL IMPLANTABLE COLLAMER LENS (VISIAN ICL)

    System, Endovascular Graft, Aortic Aneurysm Treatment

    FDA Pre-Market Approval
    FDA Class 3 ·GORE TAG THORACIC ENDOPROSTHESIS

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·Secura DR ICD, Maximo II DR ICD, Protecta XT DR ICD, Protecta DR ICD, Secura VR ICD, Maximo II VR ICD, Protecta XT VR IC

    Kit, Dna Detection, Human Papillomavirus

    FDA Pre-Market Approval
    FDA Class 3 ·BD Onclarity HPV Assay

    Drug-Eluting Peripheral Transluminal Angioplasty Catheter

    FDA Pre-Market Approval
    FDA Class 3 ·IN PACT ADMIRAL PACLITAXEL-ELUTING PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY BALLOON CATHETER