Visit us at Medica, Dusseldorf, Germany 17-20 November 2025 at Hall 16, Stand D17-5 and ask us about our free AI tools and the document builder.
Pure Global

SELF-TEST FOR GLUCOSE - ANVISA Registration 81230160010

Access comprehensive regulatory information for SELF-TEST FOR GLUCOSE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81230160010 and manufactured by manufacturer not specified. The registration is held by VISIOMED DO BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA - ME with validity until Jan 28, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including OK BIOTECH CO., LTD., ROCHE DIABETES CARE GMBH, 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
81230160010
2 Related Devices
Registration Details
ANVISA Registration Number: 81230160010
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

FAMรLIA SOLUร‡รƒO CONTROLE
Risk Class III

Registration Details

81230160010

25351729994201828

17778678000100

Dates and Status

Jan 28, 2019

28/01/2029

09/18/2025 19:00:01

FAMรLIA SOLUร‡รƒO CONTROLE
Risk Class III

Registration Details

81230160010

25351729994201828

17778678000100

Company Information

Dates and Status

Jan 28, 2019

28/01/2029

09/18/2025 19:00:01