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
- Commercial name
- AmniHook Rompedor de Membrana Amniótica Descartável
- Risk class
- Class I
PT: Rompedor de Membrana Amniotica Descartavel
Registration details
- Registration Number
- 80269330031
- Process Number
- 25351120310202395
- CNPJ
- 07424092000186
Company information
- Registration Holder
- HOSPILINE COMÉRCIO E DISTRIBUIÇÃO DE PRODUTOS MÉDICOS HOSPITALARES LTDA
- 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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