Angiotech Needle Guide

  • Modelo / Serial
    90541SRM, 90781TB4, 91061TUF, 91121TXY, 90771T9M, 90781TBE, 90981TQE, 91061TUD, 91181U2N, 91391UHZ, 91771VAV, 90851TFH, 90821TBB, 91131TYY .
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    Worldwide distribution: USA and countries of ALGERIA, ARGENTINA, AUSTRALIA, AUSTRIA, BELGIUM, BERMUDA, BRAZIL, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CZECH REPUBLIC, DENMARK, DOMINICAN REPUBLIC, ECUADOR, ESTONIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, GREECE, HONG KONG, HUNGARY, INDIA, ISRAEL, ITALY, JAPAN, KOREA, KUWAIT, LEBANON, LITHUANIA, MALAYSIA, MEXICO, MOROCCO, NETHERLANDS, NEW ZEALAND, NORWAY, PAKISTAN, PERU, PHILIPPINES, POLAND, PORTUGAL, RUSSIA, SAUDI ARABIA, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, TAIWAN, THAILAND, TURKEY, and UNITED ARAB EMIRATES.
  • Descripción del producto
    Angiotech Needle Guide. || Needle Guide for Lorad Stereo Loc. STERILE. Product Number: LNGC14GX, LNGC1619PX, LNGC2022YX, LNGO1619PX, LNGO2022YX. 510k Exempt. Qty Dist. - 13,800. || MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. || Intended Use: Needle Guide
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    Medical Device Technologies, Inc., 3600 Sw 47th Ave, Gainesville FL 32608-7555
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA