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ANVISA registration 82113060001Active

Needle Phobia Device

ANVISA Registration Number: 82113060001NOVO NORDISK FARMACÊUTICA DO BRASIL LTDANOVO NORDISK A/SRisk Class I
Verified
Device names
Technical name
Needle Phobia Device
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PT: Dispositivo Para Fobia de Agulha
Commercial name
FLEXPRO PENMATE
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Risk class
Class I
Registration details
Registration Number
82113060001
Process Number
25351205038202401
CNPJ
82277955000740
Company information
Registration Holder
NOVO NORDISK FARMACÊUTICA DO BRASIL LTDA
Manufacturer
NOVO NORDISK A/S
Manufacturing Country
Denmark
PT: DINAMARCA
Dates and status
Publication Date
May 06, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Needle Phobia Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 82113060001 and manufactured by NOVO NORDISK A/S. The registration is held by NOVO NORDISK FARMACÊUTICA DO BRASIL 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.