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ANVISA registration 80269330031Active

Disposable Amniotic Membrane Rupturer

ANVISA Registration Number: 80269330031HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDAASPEN SURGICALRisk Class I
Device names
Technical name
Disposable Amniotic Membrane Rupturer
PT: Rompedor de Membrana Amniotica Descartavel
Commercial name
AmniHook Rompedor de Membrana Amniótica Descartável
Risk class
Class I
Registration details
Registration Number
80269330031
Process Number
25351120310202395
CNPJ
07424092000186
Company information
Manufacturer
ASPEN SURGICAL
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Mar 13, 2023
Status
Active
Official value: VIGENTE
About this record

Access comprehensive regulatory information for Disposable Amniotic Membrane Rupturer in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80269330031 and manufactured by ASPEN SURGICAL. The registration is held by HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA with validity until currently active (VIGENTE).

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