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

Lancet - ANVISA Registration 80127220034

Access comprehensive regulatory information for Lancet in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80127220034 and manufactured by BOSUNG MEDITECH CO., LTD. The registration is held by PERLATENDA CONSERTO DE EQUIPAMENTOS HOSPITALARES 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 TIANJIN HUAHONG TECHNOLOGY CO., LTD., STERILANCE MEDICAL (SUZHOU) 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.

Free Database
Powered by Pure Global AI
100,000+ Devices
5 Competitors
5 Recent Registrations
80127220034
Registration Details
ANVISA Registration Number: 80127220034
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SafeLan-Pro
Risk Class I

Registration Details

80127220034

25351604892201515

01744640000179

Company Information

South Korea
PT: CORร‰IA DO SUL

Dates and Status

Nov 23, 2015

VIGENTE

09/18/2025 19:00:01