International safety notice
ESTRADIOL
Brazil / Anvisa · BRA · Jan 16, 2016
Key facts
| Title | ESTRADIOL |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | ESTRADIOL IMMULITE 2000, Kit model for 200 tests; |
| Manufacturer | DETENTOR DO REGISTRO NO BRASIL SIEMENS HEALTHCARE DIAGNÓSTICOS SA CNPJ 01449930000190 ENDEREÇO AV MUTINGA 3800 7º ANDAR PIRITUBA SÃO PAULOSP TELEFONE 0800 129 633 FABRICANTES SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LTD GLYN RHONWN LLANBERIS CAERNARFON GWYNEDD LL55 4EL REINO UNIDO SIEMENS HEALTHCARE DIAGNOSTICS INC 511 BENEDICT AVENUE TARRYTOWN NEW YORK 10591 ESTADOS UNIDOS |
| Models | 18408031, 10345161769, 93183016, 82073011, 28107022, 32682023, 24639021, 89736030, 50889027, 77559029, 54385029, 38443024 and 36 more |
| Date | Jan 16, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1