International safety notice
Technical name: Labscreen Multi HLA Class I and III and HNA
Brazil / Anvisa · BRA · May 16, 2017
Key facts
| Title | Technical name: Labscreen Multi HLA Class I and III and HNA |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Labscreen Multi HLA Class I and III and HNA Technical name: Labscreen Multi HLA Class I and III and HNA ANVISA registration number: 80298490004 Risk class: III Affected model: LSMUTR Affected serial numbers: Lot: 007 Batch: 0000091458 , 0000099706 and 0000145845 |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO BIOMETRIX DIAGNÓSTICA LTDA RUA ESTRADA DA GRACIOSA 1081 PR FABRICANTE ONE LAMBDA INC KITTRIDGE STREET 21001 CANOGA PARK CA 91303 1 818 7020042 ESTADOS UNIDOS |
| Models | 0000099706, 0000091458, 80298490004, 0000145845 |
| Date | May 16, 2017 |
| 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