International safety notice
Dressing//Curatec Hydrocolloid
Brazil / Anvisa · BRA · Jan 3, 2016
Key facts
| Title | Dressing//Curatec Hydrocolloid |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: Curatec Hydrocolloid ANVISA registration number: 80246910002 Risk class: III Affected model(s): 06 cm x 06 cm / 10 cm x 10 cm / 15 cm x 18 cm / 15 cm x 20 cm Batch(s) / Serial No(s) affected: 16081106 / 16072205 / 16072204 / 16081204 / 16090912 |
| Manufacturer | LM FARMA INDUSTRIA E COMÉRCIO LTDA CNPJ 57532343000114 RUA JAGUARÃO 95 CHÁCARAS REUNIDAS SÃO JOSÉ DOS CAMPOS SP 12 32021300 |
| Models | 16090912, 80246910002, 16072204, 16081204, 16072205, 16081106 |
| Date | Jan 3, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models 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