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

Tonometer - ANVISA Registration 80891620035

Access comprehensive regulatory information for Tonometer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80891620035 and manufactured by KEELER LTD.. The registration is held by Halma Saúde e Ótica do Brasil Importação Exportação e Distribuição Ltda with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO., LTD., TOPCON CORPORATION, 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
80891620035
Registration Details
ANVISA Registration Number: 80891620035
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Tonômetros Pulsair Keeler
Risk Class II

Registration Details

80891620035

25351414198201603

13640053000119

Company Information

KEELER LTD.
United Kingdom
PT: REINO UNIDO

Dates and Status

Nov 28, 2016

VIGENTE

09/18/2025 19:00:01