4 dispositifs dans la base de données

  • Modèle / numéro de série
  • Modèle / numéro de série
  • Description du dispositif
    "Diagnostic test strips and cassettes for urinalysis, pregnancy testing, menopause testing and opiates testing, manufactured by: IND Diagnostics Inc, Canada Alere International Ltd Barrier Healthcare Ltd E-Pharm Ltd The table below lists test strips that have been supplied in the UK between January 2011 and March 2013 Manufacturer Device Type Device Name IND Diagnostics Urinalysis Reagent Test Strips Urinalysis Reagent Test Strips IND Diagnostics HCG Pregnancy Test Indicator One-Step Urine Pregnancy Test (Cassette Format) Indicator One-Step Urine Pregnancy Test (Ministrip Format) Indicator One-Step Home Pregnancy Test (Midstream Format) Indicator One-Step Home Pregnancy Test (Mini-Midstream Format) IND Diagnostics FSH Menopause tests One Step FSH Menopause Test (Strip Format) One Step FSH Menopause Test (Cassette Format) One Step FSH Menopause Test  (Midstream Format) IND Diagnostics Opiates Test IND One Step Opiates Test Alere International Ltd. HCG Pregnancy test Axis Shield Pregnancy test dipstick and cassette Barrier Healthcare Ltd Urinalysis Reagent Test Strips DIA-CHECK Urinalysis Reagent Strips E-Pharm HCG Pregnancy Test PREGTEST (Strip format) PREGTEST (Cassette format) PREGTEST (Midstream format)"
  • Modèle / numéro de série
  • Description du dispositif
    Biokit Best 2000 laboratory analyser used in combination with the BioMerieux Vironostika HIV Uni-Form II Ag/Ab assay. The Biokit Best 2000 is also on the market as the Dynex Technologies DSX laboratory analyser. PROBLEM: The MHRA has received a report from a laboratory of an unrepeatable positive HIV test result. The positive result was not confirmed when further routine testing was carried out. The result was generated using a Biokit Best 2000 laboratory analyser in combination with the BioMerieux Vironostika HIV Uni-Form II Ag/Ab assay. The cause of the false result has not been determined. However, Biokit has stated that they have not validated this test for use on the analyser and they cannot guarantee the accuracy, reproducibility or performance of this combination. BioMerieux has stated that although the analyser meets the specifications set out in their instructions for use, this combination of assay and laboratory analyser has not been validated by them. ACTION:
  • Modèle / numéro de série
  • Description du dispositif
    Footswitches for use with all models of ConMed or Valleylab electrosurgical units (ESUs), including footswitches manufactured by third parties.

3 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Source
    BAM
  • Source
    BAM
N/A
  • Source
    FDAP