Pure Global

Buffer - ANVISA Registration 80472610004

Access comprehensive regulatory information for Buffer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80472610004 and manufactured by GENCO TIBBI CIHAZLAR SAN. TIC. LTD. STI. The registration is held by AXISTE COMÉRCIO DE PRODUTOS MÉDICOS 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 MEDTRONIC XOMED, INC., SPIGGLE & THEIS MEDIZINTECHNIK GMBH, 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
80472610004
Registration Details
ANVISA Registration Number: 80472610004
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

tampão em pva unopore com cânula
Risk Class II

Registration Details

80472610004

25351717249201917

09409545000120

Company Information

Turkey
PT: TURQUIA

Dates and Status

Apr 13, 2020

VIGENTE

09/18/2025 19:00:01