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

Connectors - ANVISA Registration 80807430046

Access comprehensive regulatory information for Connectors in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80807430046 and manufactured by ROCKET MEDICAL PLC. The registration is held by MR MEDICAL COMÉRCIO 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 BMR MEDICAL S.A., SHANGHAI HEALTH MEDICAL CO., LTD, 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
80807430046
Registration Details
ANVISA Registration Number: 80807430046
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Acoplador de guia leve Rocket® Uriglow®
Risk Class I

Registration Details

80807430046

25351698507202092

13233256000190

Company Information

ROCKET MEDICAL PLC
England (United Kingdom)
PT: INGLATERRA (REINO UNIDO)

Dates and Status

Aug 06, 2020

VIGENTE

09/18/2025 19:00:01