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

Hemostatic Forceps - ANVISA Registration 10413960247

Access comprehensive regulatory information for Hemostatic Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 10413960247 and manufactured by SCITECH PRODUTOS MEDICOS SA. The registration is held by SCITECH PRODUTOS MEDICOS SA with validity until Jun 03, 2034.

This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including SCITECH PRODUTOS MEDICOS SA, E-MED PRODUTOS MÉDICO-HOSPITALARES LTDA - ME, 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
10413960247
Registration Details
ANVISA Registration Number: 10413960247
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Pinça Bipolar Avançada Nexseal
Risk Class III

Registration Details

10413960247

25351110998202486

01437707000122

Company Information

Brazil
PT: BRASIL

Dates and Status

Jun 03, 2024

03/06/2034

09/18/2025 19:00:01