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ANVISA registration 80254180486Active

Instrumento para preparo e processamento de amostras – fase pré-analítica

ANVISA Registration Number: 80254180486PHADIA DIAGNOSTICOS LTDATHERMO ELECTRON LED GMBH ZWEIGNIEDERLASSUNG OSTERODERisk Class I
Verified
Device names
Technical name
Instrumento para preparo e processamento de amostras – fase pré-analítica
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Commercial name
Família de Centrífugas Ventiladas Séries X e S
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Risk class
Class I
Registration details
Registration Number
80254180486
Process Number
25351041280202602
CNPJ
04930429000139
Company information
Registration Holder
PHADIA DIAGNOSTICOS LTDA
Manufacturer
THERMO ELECTRON LED GMBH ZWEIGNIEDERLASSUNG OSTERODE
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Apr 13, 2026
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrumento para preparo e processamento de amostras – fase pré-analítica in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80254180486 and manufactured by THERMO ELECTRON LED GMBH ZWEIGNIEDERLASSUNG OSTERODE. The registration is held by PHADIA DIAGNOSTICOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.