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

Buffer - ANVISA Registration 80514500029

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 80514500029 and manufactured by ODHON EQUIPAMENTOS LTDA EPP. The registration is held by ODHON EQUIPAMENTOS 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 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
80514500029
Registration Details
ANVISA Registration Number: 80514500029
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

TAMPÃO NASAL ODHON
Risk Class II

Registration Details

80514500029

25351844599202099

10285608000163

Company Information

Brazil
PT: BRASIL

Dates and Status

Sep 17, 2020

VIGENTE

09/18/2025 19:00:01