International safety notice
Technical name: Procedure Glove
Brazil / Anvisa · BRA · May 11, 2017
Key facts
| Title | Technical name: Procedure Glove |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Proced Powder Free Procedure Glove Technical name: Procedure Glove ANVISA registration number: 80256170002 Risk class: I Affected model: Proced Powder Free Procedure Glove, non-sterile, smooth, ambidextrous, powder-free. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO TARGA SA CNPJ 001577740005 54 END AV IRMÃO SPINO 536 CERÂMICA PARAÍBA DO SUL RJ BRASIL CEP 25850000 FABRICANTE TARGA SA CNPJ 00157774000554 END AV IRMÃO SPINO 536 CERÂMICA PARAÍBA DO SUL RJ BRASIL CEP 25850000 |
| Models | PPFC003H, 80256170002, PPFF022G, PPFC011G, PPFF038G, PPFA001G |
| Date | May 11, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 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