International safety notice
Compresses
Brazil / Anvisa · BRA · Nov 27, 2013
Key facts
| Title | Compresses |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | HERIKA STERILE HYDROPHILIC GAUGE SURGICAL COMPRESS, lot 0155 and lot 191012G11 - registration no. 80037490003 |
| Manufacturer | AMÉRICA MEDICAL LTDA CNPJ 01310212000138 ENDEREÇO AVENIDA SAROBÁ Nº 35 BAIRRO MARIA AMÁLIA TELEFONE 38 37297427 E FAX 38 37297400 |
| Models | 191012G11, 80037490003 |
| Date | Nov 27, 2013 |
| 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