International safety notice
Technical name: Tissue Processor
Brazil / Anvisa · BRA · Jun 14, 2017
Key facts
| Title | Technical name: Tissue Processor |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Tissue Processor Technical name: Tissue Processor ANVISA registration number: 10337990010 Risk class: I Affected model: Leica ASP6025 Affected serial numbers: 321, 381, 390, 410, 436, 495, 500, 553, 559 , 597, 608, 624, 626, 657, 699, 729, 731, 733, 760, 769, 898, 939, 979, 1089, 1109 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LEICA DO BRASIL IMPORTAÇÃO E COMÉRCIO LTDA RUA JÚLIO GONZÁLES 132 15 ANDAR CONJUNTOS 92 93 E 94 BARRA FUNDA 01156060 SÃO PAULOSP 11 98923 2361 FABRICANTE LEICA BIOSYSTEMS NUSSLOCH GMBH HEIDELBERGERSTR 1719 NUSSLOCH 69226 ALEMANHA 004 962 24143345 |
| Models | ASP6025, 10337990010 |
| Date | Jun 14, 2017 |
| 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