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

Biopsy Forceps - ANVISA Registration 80014440001

Access comprehensive regulatory information for Biopsy Forceps in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80014440001 and manufactured by SCHOLTEN SURGICAL INSTRUMENTS, INC.. The registration is held by NEUROTECHS COMERCIAL 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 Jiuhong, CHANGZHOU HEALTH MICROPORT MEDICAL DEVICES 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
80014440001
Registration Details
ANVISA Registration Number: 80014440001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

SCHOLTEN NOVATOME PINÇA PARA BIÓPSIA ENDOMIOCÁRDICA
Risk Class II

Registration Details

80014440001

25351163737201047

65890170000134

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Oct 18, 2010

VIGENTE

09/18/2025 19:00:01