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ANVISA registration 10298910184Valid until Oct 21, 2034

HEMOGLOBIN SUBTYPE - NEONATAL SCREENING

ANVISA Registration Number: 10298910184REVVITY DO BRASIL LTDAWALLAC OYRisk Class III
Verified
Device names
Technical name
HEMOGLOBIN SUBTYPE - NEONATAL SCREENING
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PT: HEMOGLOBINA SUBTIPO - TRIAGEM NEONATAL
Commercial name
RESOLVE™ Hemoglobin Kit
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Risk class
Class III
Registration details
Registration Number
10298910184
Process Number
25351373258202459
CNPJ
00351210000124
Company information
Registration Holder
REVVITY DO BRASIL LTDA
Manufacturer
WALLAC OY
Manufacturing Country
Finland
PT: FINLÂNDIA
Dates and status
Publication Date
Oct 21, 2024
Validity
21/10/2034
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for HEMOGLOBIN SUBTYPE - NEONATAL SCREENING in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10298910184 and manufactured by WALLAC OY. The registration is held by REVVITY DO BRASIL LTDA with validity until Oct 21, 2034.

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.