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SPIROMETER MOUTHPIECE - ANVISA Registration 80011680038

Access comprehensive regulatory information for SPIROMETER MOUTHPIECE in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80011680038 and manufactured by WELCH ALLYN LTD.. The registration is held by WELCH ALLYN DO BRASIL, COMÉRCIO DE EQUIPAMENTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including BIOPACK PRODUTOS HOSPITALARES LTDA - EPP, MIR MEDICAL INTERNATIONAL RESEARCH S.P.A., 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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80011680038
2 Related Devices
Registration Details
ANVISA Registration Number: 80011680038
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Related Devices (2)

BOCAL DESCARTÁVEL PARA ESPIRÔMETRO
Risk Class I

Registration Details

80011680038

25351610921200891

03135603000199

Company Information

WELCH ALLYN LTD.
Ireland
PT: IRLANDA

Dates and Status

Mar 02, 2009

VIGENTE

09/18/2025 19:00:01

BOCAL DESCARTÁVEL PARA ESPIRÔMETRO
Risk Class I

Registration Details

80011680038

25351610921200891

03135603000199

Company Information

WELCH ALLYN INC.
United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Mar 02, 2009

VIGENTE

09/18/2025 19:00:01