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ANVISA registration 80269330007Active

Biopsy Device

ANVISA Registration Number: 80269330007HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDADEVICOR MEDICAL PRODUCTS INC.Risk Class II
Verified
Device names
Technical name
Biopsy Device
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PT: Dispositivo Para Biopsia
Commercial name
SONDA MAMMOTOME ELITE.
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Risk class
Class II
Registration details
Registration Number
80269330007
Process Number
25351252994201370
CNPJ
07424092000186
Company information
Registration Holder
HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA
Manufacturer
DEVICOR MEDICAL PRODUCTS INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Aug 26, 2013
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Biopsy Device in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80269330007 and manufactured by DEVICOR MEDICAL PRODUCTS INC.. The registration is held by HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES 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.