International safety notice
TUBES, GASTRO-INTESTINAL DECOMPRESSION
Brazil / Anvisa · BRA · Sep 29, 2000
Key facts
| Title | TUBES, GASTRO-INTESTINAL DECOMPRESSION |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | BARD BUTTON DECOMPRESSION TUBE EQUIPMENT (BARD BUTTON DEVICE DECOMPRESSION TUBES): (FROM 1 TO 24) 18 FR, (FROM 1 TO 24) 24 FR, (FROM 1 TO 24) 28 FR; |
| Manufacturer | BARD INTERVENTIONAL PRODUCTS DIV C R BARD INC 107154 129 CONCORD RD BLDG 3 PO BOX 7031 BILLERICA MA 018217031 DISTRIBUIDOR C R BARD INC 150057 730 CENTRAL AVE MURRAY HILL NJ 079741139 FABRICANTE |
| Models | 000351, 000282, 000358, 000292, 000296, 000286, 000357, 000355, 000354, 000261, 000352, 000285 and 10 more |
| Date | Sep 29, 2000 |
| 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