International safety notice
BALLOON CATHETER FOR THERMACHOICE III UTERINE THERAPY SYSTEM
Brazil / Anvisa · BRA · Dec 28, 2015
Key facts
| Title | BALLOON CATHETER FOR THERMACHOICE III UTERINE THERAPY SYSTEM |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | - Nome comercial: GYNECARE THERMACHOICE™ III Thermal Balloon Ablation Silicone Catheter - ANVISA registration number: 10132590446 - Risk class: II - Medium Risk - Model(s) affected; |
| Manufacturer | DADOS DO DETENTOR DO REGISTRO DO PRODUTO NO BRASIL NOME JOHNSON JOHNSON DO BRASIL IND E COM DE PROD PARA SAÚDE LTDA CNPJ 54516661000101 ENDEREÇO RUA GERIVATIBA 207 MUNICÍPIOUF SÃO PAULOSP TELEFONE DE CONTATO 55 12 39327977 PRODUTOS FABRICADOS NO EXTERIOR NOME DA EMPRESA FABRICANTE GYNECARE INC ENDEREÇO MUNICÍPIO PAÍS ESTADOS UNIDOS DA AMÉRICA |
| Models | HPMG03, HGMG02, GLMG09, HBMG05, HLMG06, HEMG01, TC033, 10132590446, HDMG01, HMMG01, GPMG01, HBMG09 |
| Date | Dec 28, 2015 |
| 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