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

Instrument Kit - ANVISA Registration 80240599001

Access comprehensive regulatory information for Instrument Kit in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80240599001 and manufactured by TORNIER SAS - ETABLISSEMENT BIOPROFILE. The registration is held by ORTECH MEDICAL COMERCIO IMPORTAÇÃO E EXPORTAÇÃO LTDA/EPP 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 MARDEN MEDICAL LTDA, LIMA CORPORATE S.P.A, 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
80240599001
Registration Details
ANVISA Registration Number: 80240599001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Kit de Provas para APSI
Risk Class I

Registration Details

80240599001

25351047765201213

06328384000152

Company Information

France
PT: FRANÇA

Dates and Status

Mar 12, 2012

VIGENTE

09/18/2025 19:00:01