International safety notice
REAGENTS, ROTAVIRUS DETECTION REAGENTS, ENZYME IMMUNOASSAY
Brazil / Anvisa · BRA · Jul 20, 2000
Key facts
| Title | REAGENTS, ROTAVIRUS DETECTION REAGENTS, ENZYME IMMUNOASSAY |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | IMMUNOCARD ROTAVIRUS ENZYME-LINKED IMMUNOSORBENT ASSAY TEST KITS: PRODUCT NO. 708030; LOT NOS.: 708030.139, A .142, .145 |
| Manufacturer | MERIDIAN DIAGNOSTICS INC 105832 3471 RIVER HILLS DR CINCINNATI OH 452443023 |
| Models | 708030, 708030.139 |
| Date | Jul 20, 2000 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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