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Gastrostomy Kit - ANVISA Registration 80102513180

Access comprehensive regulatory information for Gastrostomy Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102513180 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Jan 15, 2034.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including HANGZHOU FUSHAN MEDICAL APPLIANCES CO. LTD., AVANOS MEDICAL, INC., and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

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80102513180
2 Related Devices
Registration Details
ANVISA Registration Number: 80102513180
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Related Devices (2)

KIT PARA GASTROSTOMIA ENDOSCÓPICA PERCUTÂNEA (GEP) MIC* ENFIT
Risk Class III

Registration Details

80102513180

25351220222202392

04718143000194

Dates and Status

Jan 15, 2024

15/01/2034

09/18/2025 19:00:01

KIT PARA GASTROSTOMIA ENDOSCÓPICA PERCUTÂNEA (GEP) MIC* ENFIT
Risk Class III

Registration Details

80102513180

25351220222202392

04718143000194

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Jan 15, 2024

15/01/2034

09/18/2025 19:00:01