International safety notice
Alert 2729 (Technosurveillance) - Endoclear Eq. Med.
Brazil / Anvisa · BRA · Nov 9, 2018
Key facts
| Title | Alert 2729 (Technosurveillance) - Endoclear Eq. Med. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade Name: Endoclear Technical Name: Digestive Endoscope Cleaning/Disinfection Device ANVISA registration number: 80316870002 Risk Class: II Affected model: ALX 1012 DL Affected serial numbers: see attachment "Lots at risk" |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ENDOCLEAR EQUIPAMENTOS MÉDICOS HOSPITALARES LTDA CNPJ 54907449000167 AVENIDA ALBERTO PULICANO 4110 DISTRITO INDUSTRIAL FRANCA SP TEL 016 37071200 EMAIL HENRIQUEENDOCLEARCOMBR FABRICANTE DO PRODUTO ENDOCLEAR EQUIPAMENTOS MÉDICOS HOSPITALARES LTDA CNPJ 54907449000167 AVENIDA ALBERTO PULICANO 4110 DISTRITO INDUSTRIAL FRANCA SP TEL 016 37071200 EMAIL HENRIQUEENDOCLEARCOMBR |
| Models | 80316870002 |
| Date | Nov 9, 2018 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
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