IMMUNOHEMATOLOGY - ABO - HUMAN ORIGIN - ANVISA Registration 80155020032
Access comprehensive regulatory information for IMMUNOHEMATOLOGY - ABO - HUMAN ORIGIN in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 80155020032 and manufactured by programa nacional de controle de qualidade ltda. The registration is held by programa nacional de controle de qualidade ltda with validity until Apr 24, 2033.
This page provides complete technical specifications for this device, regulatory compliance details, 5 companies making the same product including DIAGNOSTIC GRIFOLS, S.A., DIAGNOSTIC GRIFOLS 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
80155020032
25351560099202269
73302879000108
Company Information
Dates and Status
Apr 24, 2023
24/04/2033
09/18/2025 19:00:01
IMUNOHEMATOLOGIA - ABO - ORIGEM HUMANA
Kit IBMP TR ABO/Rh
INSTITUTO DE BIOLOGIA MOLECULAR DO PARANÁ
80780040019
Sep 25, 2023
IMUNOHEMATOLOGIA - ABO - ORIGEM HUMANA
Família Reverse-Cyte® 5%
Not specified
80134860273
Dec 28, 2020
IMUNOHEMATOLOGIA - ABO - ORIGEM HUMANA
Família Reverse-Cyte® 5%
MEDION DIAGNOSTICS GRIFOLS AG
80134860273
Dec 28, 2020
IMUNOHEMATOLOGIA - ABO - ORIGEM HUMANA
Reverse-Cyte 0.8%
Not specified
80134860269
Nov 25, 2019
IMUNOHEMATOLOGIA - ABO - ORIGEM HUMANA
Reverse-Cyte 0.8%
MEDION GRIFOLS DIAGNOSTICS AG
80134860269
Nov 25, 2019

