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ANVISA registration 80048490106Valid until Jan 05, 2036

PROSTATE-SPECIFIC ANTIGEN (PSA)

ANVISA Registration Number: 80048490106USA DIAGNOSTICA LTDAMONOBIND, INCRisk Class III
Device names
Technical name
PROSTATE-SPECIFIC ANTIGEN (PSA)
PT: ANTÍGENO PROSTÁTICO ESPECÍFICO (PSA)
Commercial name
PSA Total Test System - ELISA
Risk class
Class III
Registration details
Registration Number
80048490106
Process Number
25351108656202587
CNPJ
02330159000108
Company information
Registration Holder
USA DIAGNOSTICA LTDA
Manufacturer
MONOBIND, INC
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
Jan 05, 2026
Validity
05/01/2036
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for PROSTATE-SPECIFIC ANTIGEN (PSA) in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 80048490106 and manufactured by MONOBIND, INC. The registration is held by USA DIAGNOSTICA LTDA with validity until Jan 05, 2036.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.