International safety notice
Technical name: Disc replacement interbody spacing device
Brazil / Anvisa · BRA · Nov 22, 2016
Key facts
| Title | Technical name: Disc replacement interbody spacing device |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Nome comercial: Kage Cervical // Technical name: Disc replacement interbody spacing device // ANVISA registration number: 80240590034 // Risk class: III - High Risk // Affected model: KAG04 // Affected batch number: 467/025-1 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO ORTECH MEDICAL COM IMP EXP LTDA RUA JORGE AUGUSTO 83 SALAS 55 A 58 SÃO PAULOSP ORTECHTERRACOMBR 11 25323710 FABRICANTE KASIOS 18 CHEMIN DE LA VIOLETTE 31240 L UNION FRANCE |
| Models | KAG04, 025-1, 80240590034 |
| Date | Nov 22, 2016 |
| 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