CA 50 ANTIGEN - ANVISA Registration 80102512903
Access comprehensive regulatory information for CA 50 ANTIGEN in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80102512903 and manufactured by manufacturer not specified. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until Nov 16, 2032.
This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 similar products found using AI-powered semantic search, 1 companies making the same product including AUTOBIO DIAGNOSTICS CO., LTD, and 2 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.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Contact Pure Global Brazil TeamRelated Devices (2)
Registration Details
80102512903
25351229806202242
04718143000194
Company Information
Dates and Status
Nov 16, 2022
16/11/2032
09/18/2025 19:00:01
CA 50 ANTIGEN
FAMILIA AUTOLUMO CA50 MICROPARTÍCULAS (CLIA)
Not specified
80102513433
May 19, 2025
CA 50 ANTIGEN
FAMILIA AUTOLUMO CA50 MICROPARTÍCULAS (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513433
May 19, 2025
CA 72-4 ANTIGEN
FAMILIA MAGLUMI CA 72-4 (CLIA)
Not specified
80102512900
Nov 16, 2022
CA 72-4 ANTIGEN
FAMILIA MAGLUMI CA 72-4 (CLIA)
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
80102512900
Nov 16, 2022
CARCINOEMBRYONIC ANTIGEN
FAMILIA MAGLUMI CEA (CLIA)
Not specified
80102512907
Nov 21, 2022
ANTÍGENO CA 50
FAMILIA AUTOLUMO CA50 MICROPARTÍCULAS (CLIA)
Not specified
80102513433
May 19, 2025
ANTÍGENO CA 50
FAMILIA AUTOLUMO CA50 MICROPARTÍCULAS (CLIA)
AUTOBIO DIAGNOSTICS CO., LTD
80102513433
May 19, 2025