CRYPTOCOCCUS NEOFORMANS - ANVISA Registration 80954880175
Access comprehensive regulatory information for CRYPTOCOCCUS NEOFORMANS in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80954880175 and manufactured by Eco Diagnostica Ltda. The registration is held by Eco Diagnostica Ltda with validity until Aug 16, 2031.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including REMEL INC, BIOSYNEX S.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.
Device Details
Registration Details
80954880175
25351727759202117
14633154000206
Company Information
Dates and Status
Aug 16, 2021
16/08/2031
09/18/2025 19:00:01
REMEL INCโข United States of America
BIOSYNEX S.A.โข France
ALAMAR TECNO CIENTรFICA LTDAโข Brazil
IMMY INCโข United States of America
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDAโข Brazil
CRYPTOCOCCUS NEOFORMANS
FASTLINE CRYPTOCOCCUS Ag
KHAYROS DIAGNOSTICA FABRICACAO, COMERCIALIZACAO E DISTRIBUICAO DE PRODUTOS LTDA
80105220179
Mar 11, 2024
CRYPTOCOCCUS NEOFORMANS
CrAg Lateral Flow Assay
IMMY INC
81504790240
Oct 13, 2020
CRYPTOCOCCUS NEOFORMANS
CrAg Lateral Flow Assay
Not specified
81504790240
Oct 13, 2020
CRYPTOCOCCUS NEOFORMANS
Biosynexยฎ CryptoPS
Not specified
80686360294
Aug 17, 2020
CRYPTOCOCCUS NEOFORMANS
Biosynexยฎ CryptoPS
BIOSYNEX S.A.
80686360294
Aug 17, 2020

