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

Automated external defibrillator - ANVISA Registration 10216710313

Access comprehensive regulatory information for Automated external defibrillator in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10216710313 and manufactured by PHILIPS GOLDWAY (SHENZHEN) INDUSTRIAL INC.. The registration is held by PHILIPS MEDICAL SYSTEMS LTDA with validity until Oct 20, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including ZOLL MEDICAL CORPORATION, Instramed Industria Médico Hospitalar LTDA, 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
10216710313
2 Related Devices
Registration Details
ANVISA Registration Number: 10216710313
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Related Devices (2)

Desfibrilador/Monitor Efficia
Risk Class IV

Registration Details

10216710313

25351375783201507

58295213000178

Company Information

China
PT: CHINA, REPÚBLICA POPULAR

Dates and Status

Oct 20, 2015

20/10/2035

09/18/2025 19:00:01

Desfibrilador/Monitor Efficia
Risk Class IV

Registration Details

10216710313

25351375783201507

58295213000178

Company Information

Dates and Status

Oct 20, 2015

20/10/2035

09/18/2025 19:00:01