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 NEEDLE - ANVISA Registration 80142340036

Access comprehensive regulatory information for BIOPSY NEEDLE in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80142340036 and manufactured by HS HOSPITAL SERVICE S.P.A. The registration is held by ADEF RIO MATERIAL HOSPITALAR 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 STERYLAB S.R.L., ZHEJIANG CURAWAY MEDICAL TECHNOLOGY 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
80142340036
Registration Details
ANVISA Registration Number: 80142340036
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

KIT DE BIÓPSIA DE MEDULA ÓSSEA HS TRAPSYSTEM
Risk Class II

Registration Details

80142340036

25351456557201532

36193514000158

Company Information

Italy
PT: ITÁLIA

Dates and Status

Aug 31, 2015

VIGENTE

09/18/2025 19:00:01