GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR - ANVISA Registration 81506640019

Access comprehensive regulatory information for GENERAL PURPOSE GUIDE WIRE, NON-VASCULAR in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 81506640019 and manufactured by BIÇAKCILAR TIBBI CIHAZLAR SANAYI A.S.. The registration is held by ONCORMED PRODUTOS PARA SAÚDE LTDA - ME with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including BOSTON SCIENTIFIC CORPORATION, BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED, 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 Similar Products
5 Competitors
81506640019
Registration Details
ANVISA Registration Number: 81506640019
Janaina dos Santos de Miranda

Janaina dos Santos de Miranda

🇧🇷 Brazil Regulatory Expert

Need help with your Brazil registration?

Contact Pure Global Brazil Team
Free consultation

Device Details

ESTILETE DE INTUBAÇÃO PARA SONDA ENDOTRAQUEAL
Risk Class I

Registration Details

81506640019

25351440722202187

20088885000130

Company Information

Turkey
PT: TURQUIA

Dates and Status

May 13, 2021

VIGENTE

09/18/2025 19:00:01