International safety notice
Sphincter implant.
Brazil / Anvisa · BRA · Jun 20, 2011
Key facts
| Title | Sphincter implant. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | AMS 800 URINARY CONTROL DEVICE. Anvisa registration: 80219980027. Model: Standard Control Pump (72400098). |
| Manufacturer | DETENTOR DO REGISTRO AMS AMERICAN MEDICAL SYSTEMS PROD URINÁRIOS E GINECOLÓGICOS LTDA AV IBIRAPUERA 2907 CONJ 1212 SÃO PAULOSP TEL 11 50919753 FAX 11 50539709 EMAIL JULIANADOSSANTOSAMMDCOM |
| Models | 72400098, 80219980027 |
| Date | Jun 20, 2011 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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