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ANVISA registration 81420890051Active

Instrumentation For Endoscopy

ANVISA Registration Number: 81420890051MEDIC DISTRIBUIDORA DE EQUIPAMENTOS MEDICOS LTDA - EPPDOPPKON GMBH & CO. KGRisk Class I
Verified
Device names
Technical name
Instrumentation For Endoscopy
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PT: Instrumental Para Endoscopia
Commercial name
Spineedle Titanium Guidewire
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Risk class
Class I
Registration details
Registration Number
81420890051
Process Number
25351459743202419
CNPJ
08049999000175
Company information
Registration Holder
MEDIC DISTRIBUIDORA DE EQUIPAMENTOS MEDICOS LTDA - EPP
Manufacturer
DOPPKON GMBH & CO. KG
Manufacturing Country
Germany
PT: ALEMANHA
Dates and status
Publication Date
Jan 13, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Instrumentation For Endoscopy in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81420890051 and manufactured by DOPPKON GMBH & CO. KG. The registration is held by MEDIC DISTRIBUIDORA DE EQUIPAMENTOS MEDICOS LTDA - EPP 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.