Devices

DrugCheck

  • Modèle / numéro de série
    134268 134898 140206 140218 140453 140551 141053 141129 143471 143553 144468 144557 150317 150531 150606 150638 150834 151154 152021 152104 134067 134504 140495 141010 141128 141197 143716 143784 143866 144003 144042 144199 144270 144332 144443 144502 144555 150237 150347 150440 150901 150989 151239 151925 151984 152003 152103
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution - US (nationwide) and Internationally to Australia.
  • Description du dispositif
    EDI BZO UNCUT SHEET-CARD, Item No. 100170 || These Drugs of Abuse Tests are one-step immunoassays for the qualitative detection of multiple drugs and drug metabolites in human urine. The configurations of these Drugs of Abuse Tests consist of a combination of drug strips, including Benzodiazepine (BZO). They are used to obtain a visual, qualitative result and are intended for professional and point of care use.
  • Manufacturer
    Ameditech Inc
  • 1 Event

Fabricant

Ameditech Inc
  • Adresse du fabricant
    Ameditech Inc, 9940 Mesa Rim Rd, San Diego CA 92121-2910
  • Source
    USFDA

17 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

DRUGCHECK
  • Modèle / numéro de série
  • Description du dispositif
    in-vitro_medical_device
  • Manufacturer
    ALL DIAG
Device Recall DrugCheck Drugs of Abuse Ketamine Dip Test
  • Modèle / numéro de série
    PC 09077, PC03227, PC03055, PC09293, PC11115, PC08126, PC06276, PC07085, PC06305, and PC08017.
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    3
  • Dispositif implanté ?
    No
  • Distribution
    Worldwide Distribution -- US, including the states of CA, NY, MN, and SC; SWEDEN, CANADA, UNITED KINGDOM, and GUATEMALA.
  • Description du dispositif
    DrugCheck Ketamine Dip Test || 31317-3P PRO-EU-SWE, 31226-3-CA-GML, 30842 TR, 30108C, 30108C CAN, 30108C EU, and 30108C INT. || This assay provides only a preliminary analytical test result.
  • Manufacturer
    Express Diagnostics Int'l., Inc.
Device Recall ProScreen, DrugSmart, DrugCheck, Immutest
  • Modèle / numéro de série
    151688 152423 153307 153912 153921 153961 153962 154104 154112 154236 154264
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    12-Panel Dip Drug Screen with adulterant, Item No. PSDA-12BUP, PSD-6MTDBO300, PSD-10PPX, PSD-10MOX, 60960D, 61127D, DCC-81205-5, || IMCA-10M5.
  • Manufacturer
    Ameditech Inc
Device Recall DrugCheck
  • Modèle / numéro de série
    143235 144216 151591 153132 153489
  • Classification du dispositif
    Clinical Chemistry and Clinical Toxicology Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    DrugCheck Waived 12 Panel Cup w/Adult, Item No. DCC-81205-5
  • Manufacturer
    Ameditech Inc
DrugCheck 3 Test Cup COC/MET/THC || Product Code 60300
12 en plus