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NEISSERIA SP - ANVISA Registration 10033430774

Access comprehensive regulatory information for NEISSERIA SP in Brazil's medical device market through Pure Global AI's free database. This Risk Class IV medical device is registered under ANVISA number 10033430774 and manufactured by BECTON, DICKINSON AND COMPANY. The registration is held by BECTON DICKINSON INDÚSTRIAS CIRÚRGICAS LTDA. with validity until Apr 15, 2029.

This page provides complete technical specifications for 2 related devices, regulatory compliance details, 5 companies making the same product including QIAGEN, GUANGZHOU WONDFO BIOTECH CO. LTD, 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.

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10033430774
2 Related Devices
Registration Details
ANVISA Registration Number: 10033430774
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Related Devices (2)

BD ProbeTec™ Neisseria gonorrhoeae (GC) QX Assay Gray Amp Reagent Pack
Risk Class IV

Registration Details

10033430774

25351089290201991

21551379000106

Company Information

United States of America
PT: ESTADOS UNIDOS DA AMÉRICA

Dates and Status

Apr 15, 2019

15/04/2029

09/18/2025 19:00:01

BD ProbeTec™ Neisseria gonorrhoeae (GC) QX Assay Gray Amp Reagent Pack
Risk Class IV

Registration Details

10033430774

25351089290201991

21551379000106

Company Information

Dates and Status

Apr 15, 2019

15/04/2029

09/18/2025 19:00:01