Life Technologies Corporation

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 4 건

  • 모델명 / 제조번호(시리얼번호)
    Catalog #18081020, Lot #1368760 & Lot #1312093
  • 의료기기 분류등급
  • 의료기기 등급
    3
  • 이식된 장치?
    No
  • 유통
    USA Nationwide Distribution in the states of DE, IA, MN, and NC.
  • 제품 설명
    HSV 2 Primers, Catalog #18081020. Analyte Specific Reagent. The HSV-2 primer pair is specific for HSV-2 (Herpes Simplex Virus 2). For use in Clinical laboratories when developing their own diagnostic tests.
  • 모델명 / 제조번호(시리얼번호)
    Lot 1705001 UDI: (01)10190302006385(17)180220(10)1705001(240)A32441
  • 의료기기 분류등급
  • 의료기기 등급
    3
  • 이식된 장치?
    No
  • 유통
    Distributed to states: AZ, CA, NC, TX, and VA.
  • 제품 설명
    Oncomine Dx Target Test, (Model No. A32451), Oncomine Dx Target RNA/DNA Panel (Model No. A32441). || A qualitative In Vitro Diagnostic test.
  • 모델명 / 제조번호(시리얼번호)
    Model # MHFH01 UDI (01)10190302005579(17)180430 (10)1626670D(240)MHFH01  Lot# 1626670D  Model # MHFH01 UDI (01)10190302005579(17)190830 (10)1873068B(240)MHFH01 Lot# 1873068B  Model # MHFH01 UDI (01)10190302005579(17)191030 (10)1915224B(240)MHFH01  Lot# 1915224B
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    MI, CA, IL, TX, SC, NY, MN, DE, NJ, WA , OR, IN, MA, DE, FL, PA
  • 제품 설명
    Human Fetal Hemoglobin (HBF-1) FITC Conjugate
  • 모델명 / 제조번호(시리얼번호)
    Lot Numbers: v1.8 (Rev. C) (REVC20170906) and v1.8 (Rev. C) (REVC27JUN2017)  UDI: (01)10190302006071
  • 의료기기 분류등급
  • 의료기기 등급
    3
  • 이식된 장치?
    No
  • 유통
    US Distribution to the states of: AZ, CA, NC, TX, and VA.
  • 제품 설명
    Oncomine Dx Target Test User Guides and Assay Definition File, Model: A32461; UDI: (01)10190302006071(11)170911(10)1.8(240)A32461 || The Oncomine Dx Target Test is a qualitative in vitro diagnostic test that uses targeted high- throughput, parallel-sequencing technology to detect single-nucleotide variants (SNVs) and deletions in 23 genes from DNA and fusions in ROS1 from RNA isolated from formalin-fixed, paraffin-embedded (FFPE) tumor tissue samples from patients with non-small cell lung cancer (NSCLC) using the Ion PGM Dx System. The test is indicated to aid in selecting NSCLC patients for treatment with the targeted therapies listed in Table 1 in accordance with the approved therapeutic product labeling.

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 9 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 주소
    Life Technologies Corporation, 7305 Executive Way, Frederick MD 21704-8354
  • 제조사 모회사 (2017)
  • Source
    USFDA
하나 더 4 건 더