International safety notice
Alert 2624 (Technosurveillance) Lab. B. Braun S.A. - Celsite - Intraspinal Access Port;
Brazil / Anvisa · BRA · Jul 23, 2018
Key facts
| Title | Alert 2624 (Technosurveillance) Lab. B. Braun S.A. - Celsite - Intraspinal Access Port; |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial Name: Celsite - Intraspinal Access Port; Technical Name: Catheters; ANVISA registration number: 80136990518; Classe de Risco: IV (80136990518); Modelo afetado: CELSITE ST304-19 ST SET PA/PUR 19G E/S; PERIFIX 300 BASIC SET; PERIFIX 310 BASIC SET; PERIFIX CATETER 0.45X0.85, 20G; PERIFIX CATETER 0.60X1.05, 19G; ESPOCAN D.S. COM SPINOCAN G27; ESPOCAN D.S. COM PENCAN G27; CONJUNTO CONTIPLEX TUOHY 1.3X100MM 18G Números de série afetados: Celsite Intraesp. ST304-19G 38 x 26 x 1: 36928547 / CONJUNTO CONTIPLEX TUOHY 1.3X100MM 18G: 17L16A8701, 18A30A8701 / ESPOCAN D.S. COM PENCAN G27: 17K06A8701, 17K07A8701, 17N05A8701, 17N18A8701, 18B12A8701, 18B22A8701 / ESPOCAN D.S. COM SPINOCAN G27: 17K22A8701, 18A08A8701 / PERIFIX 300 BASIC SET: 17K29A8701, 18A15A8701 / PERIFIX 310 BASIC SET: 17K20A8701, 17M16A8701, 18C16A8701 / PERIFIX CATETER 0.45X0.85, 20G: 17K14A8701, 17M14A8701, 18A12A8701, 18B19A8701 / PERIFIX CATETER 0.60X1.05, 19G: 17K15A8701, 17N13A8701, 18A24A8701. |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO LABORATÓRIOS B BRAUN SA CNPJ 31673254000102 AV EUGÊNIO BORGES 1092 E AV JEQUITIBÁ 9 CEP 24751000 SÃO GONÇALO RJ TEL 55 21 26023219 EMAIL ROSANERAMOSBBRAUNCOM FABRICANTE DO PRODUTO B BRAUN MELSUNGEN AG 34209 MELSUNGEN ALEMANHA |
| Models | 17K07A8701, 17K06A8701, 10008530058, 18A24A8701, 18A30A8701, 17K29A8701, 0.60X1.05, 17K22A8701, 80136990462, ST304-19, 17M16A8701, 18B22A8701 and 20 more |
| Date | Jul 23, 2018 |
| 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