Binax, Inc. dba IMPD

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 5 건

  • 모델명 / 제조번호(시리얼번호)
    Lot number: 24162
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide and Japan.
  • 제품 설명
    BinaxNOW A&B; Kit 10 Test Kit (Japan) || Part No. 416-110J contains NP Swabs with '8995' labeled on the swab wrapper
  • 모델명 / 제조번호(시리얼번호)
    Kit lot Numbers: 023357, 023566, 024629, 024631,
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide and Japan.
  • 제품 설명
    BinaxNOW Nasopharyngeal (NP) Accessory Pak, Part Number 400-065, contain NP Swabs with '8995' labeled on the swab wrapper
  • 모델명 / 제조번호(시리얼번호)
    Kit Lot Numbers: 023437, 024056, 024057, 024436, 024516, 024518, 024694, 024695, 024882, 025090, 025089 NP Swabs Lot Number: 8995
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide and Japan.
  • 제품 설명
    BinaxNOW RSV 10 Test Kit || Part Number : 430-100, contains NP Swabs with '8995' labeled on the swab wrapper
  • 모델명 / 제조번호(시리얼번호)
    Kit Lot Numbers:024020, 024175, 024360, 024361, 024385, 024596, 024597, 024703, 024705, 024704, 024714, 024715, 024718, 024726, 025087 NP Swabs Lot Number: 8995
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide and Japan.
  • 제품 설명
    BinaxNOW Influenza A&B; 22 Test Kit || Part Number: 416-022, contains NP Swabs with '8995' labeled on the swab wrapper
  • 모델명 / 제조번호(시리얼번호)
    Kit Lot Numbers: 023378, 023411, 023433, 023616, 024021, 024384, 024479, 024480, 024622 NP Swabs Lot Number: 8995
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Nationwide and Japan.
  • 제품 설명
    BinaxNOW Influenza A&B; 10 Test KIT || Part Number: 416-110 contains NP Swabs with '8995' labeled on the swab wrapper

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데이터에 대해 더 자세히 알아보기 여기

  • 제조사 주소
    Binax, Inc. dba IMPD, 10 Southgate Rd, Scarborough ME 04074
  • 제조사 모회사 (2017)
  • 제조사 의견
    “We are in constant communication with regulatory agencies and competent authorities worldwide which allows us to implement global recalls or in-country communication quickly and effectively,” Abbott, which now owns St. Jude Medical told ICIJ in a statement. In addition to sending global notices to physicians worldwide, we also make sure that product advisories are available online and classification of product recalls and product advisories are determined by global regulatory bodies which can impact the timing in any given country. MD companies follow varying regulations in different countries. In come countries software is not regulated so a recall in one country related to software would not be classified as a recall or field action in another. In addition, review cycles within the regulatory process can be different in each country which can impact communication and recall timing.
  • Source
    USFDA