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

SPACER FOR OTORHINOLARYNGOLOGY - ANVISA Registration 80978870001

Access comprehensive regulatory information for SPACER FOR OTORHINOLARYNGOLOGY in Brazil's medical device market through Pure Global AI's free database. This Risk Class I medical device is registered under ANVISA number 80978870001 and manufactured by CIPLA LIMITED. The registration is held by CIPLA BRASIL IMPORTADORA E DISTRIBUIDORA DE MEDICAMENTOS LTDA with validity until currently active (VIGENTE).

This page provides complete technical specifications for this device, regulatory compliance details, 1 companies making the same product including OSCIMED SA, and 1 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
1 Competitors
1 Recent Registrations
80978870001
Registration Details
ANVISA Registration Number: 80978870001
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Free consultation

Device Details

Registration Details

80978870001

25351258640202018

18268051000164

Company Information

CIPLA LIMITED
India
PT: รNDIA

Dates and Status

Oct 29, 2020

VIGENTE

09/18/2025 19:00:01

Companies Making Similar Products
Top companies providing products with the same technical name: "SPACER FOR OTORHINOLARYNGOLOGY"
Recent Registrations
Recently registered products with the same technical name: "SPACER FOR OTORHINOLARYNGOLOGY"