International safety notice
Disposable Syringes
Brazil / Anvisa · BRA · May 6, 2016
Key facts
| Title | Disposable Syringes |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name of the product: SINGLE-USE STERILE HYPODERMIC SYRINGE WITH DL NEEDLE /// Registration number: 80511919003 /// Affected model(s): 3 and 5 mL/// affected batch: 1408-05 and 1408- 01/// Product risk class: II |
| Manufacturer | DETENTOR DO REGISTRO DLP MEDICAL DO BRASIL INDÚSTRIA E COMÉRCIO LTDA CNPJ 10460361000174 ENDEREÇO RUA JOSE MEDEIROS E ALBUQUERQUE 413 TABOAO SP TEL 11 2669 6235 FABRICANTES DL MÉDICA SA DE CV MÉXICO |
| Models | 80511919003, 1408-05, 1408-01 |
| Date | May 6, 2016 |
| 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