À propos de cette base de données
Comment utiliser cette base de données
Téléchargez les données
FAQ
Crédits
Devices
Device Recall ADVIA Centaur Systems TSH3 Ultra ReadyPack
Modèle / numéro de série
Per recall strategy.
Classification du dispositif
Clinical Chemistry and Clinical Toxicology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide Distribution-USA (nationwide) and the countries of Canada, AE, AR, AT, AU, BA, BD, BE, BG, BO, BR, BY, CH, CL, CM, CN, CO, CR, CY, CZ, DE, DK, DO, DZ, EC, EE, EG, ES, FI, FR, GB, GR, GT, HK, HN, HR, HU, ID, IE, IL, IN, IR, IS, IT, JO, JP, KA, KR, KW, KZ, LB, LK, LT, LV, LY, MA, MK, MT, MX, MY, NI, NL, NO, NP, OM, PA, PE, PH, PK, PL, PT, PY, QA, RO, RU, SA, SE, SG, SK, SV, SY, TH, TM, TN, TR, TW, UA, UY, UZ, VE, VN, XS, and ZA.
Description du dispositif
ADVIA Centaur Systems TSH3 Ultra ReadyPack ((REF 06491072 - 100 Tests, REF 06491080 - 500 Tests, REF 04862625 - 2500T). || Intended to quantitatively measure human thyroid stimulating hormone (TSH, thyrotropin).
Manufacturer
Siemens Healthcare Diagnostics, Inc
1 Event
Rappel de Device Recall ADVIA Centaur Systems TSH3 Ultra ReadyPack
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Fabricant
Siemens Healthcare Diagnostics, Inc
Adresse du fabricant
Siemens Healthcare Diagnostics, Inc, 333 Coney St, East Walpole MA 02032-1516
Société-mère du fabricant (2017)
Siemens Ag
Source
USFDA
Language
English
Français
Español
한국어