International safety notice
Technical name: BALLOON CATHETER FOR CORONARY ANGIOPLASTY (9000005)
Brazil / Anvisa · BRA · Mar 20, 2017
Key facts
| Title | Technical name: BALLOON CATHETER FOR CORONARY ANGIOPLASTY (9000005) |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: NC TREK RX CORONARY DILATATION CATHETER Technical name: BALLOON CATHETER FOR CORONARY ANGIOPLASTY (9000005) ANVISA registration number: 80146501766 Risk class: IV Affected model: 1012444-06, 1012444-08, 1012444-12, 1012444-1 5, 1012444-20, 1012445-06, 1012445-08, 1012445-12, 1012445-15, 1012445-20, 1012446-06, 1012446-08, 1012446-12, 1012446-15, 1 012446-20, 1012447-06, 1012450- 08, 1012447-12, 1012447-15, 1012447-20, 1012447-25, 1012448-06, 1012448-08, 1012448-12, 1012448-15, 1012448-20, 1012449-0 6, 1012449-08, 1012449-12, 1012449-15, 1012449-20, 1012449-25, 1012450-06, 1012450-08, 1012450-12, 1012450-15, 1012450-20, 1012451-06, 1012451-08, 1 012451-12, 1012451-15, 1012451- 20, 1012451-25, 1012452-08, 1012452-12, 1012452-15, 1012452-20, 1012453-08, 1012453-12, 1012453-15, 1012453-20, 1012454-0 8, 1012454-12, 1012454-15, 1012454-20, 1012455-08, 1012455-12, 1012455-15, 1012455-20. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ABBOTT LABORATÓRIOS DO BRASIL LTDA RUA MICHIGAN 735 BROOKLIN CEP 04566905 SÃO PAULO FABRICANTE ABBOTT VASCULAR 3200 LAKESIDE DRIVE SANTA CLARA CA 95054 EUA |
| Models | 1012449-20, 1012455-12, 1012452-12, 1012449-06, 1012453-12, 9000005, 1012447-12, 1012453-08, 1012444-12, 1012446-12, 1012445-08, 1012449-12 and 48 more |
| Date | Mar 20, 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