International safety notice
Lasma Deficient in Coagulation Factors
Brazil / Anvisa · BRA · Jul 24, 2017
Key facts
| Title | Lasma Deficient in Coagulation Factors |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Trade name: FACTOR XII DEFICIENT PLASMA HEMOSIL 10 X 1 mL - 10 x 1 mL Technical name: Lasma Deficient in Coagulation Factors ANVISA registration number: 80003610279 Risk class: II Affected model: N/A Affected serial numbers: N958653 (06 units), N261273 (42 units) |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO WERFEN MEDICAL LTDA CNPJ 02004662000165 ESTRADA DOS ROMEIROS KM 385 CONDOMÍNIO MORRO GRANDE MÓD G9 N 138 SANTANA DE PARNAÍBA SP FABRICANTE INSTRUMENTATION LABORATORY 180 HARTWELL ROAD BEDFORD MA 017302443 ESTADOS UNIDOS EMAIL RAITMAILILWWIT |
| Models | N261273, 80003610279, N958653 |
| Date | Jul 24, 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