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GLUTAMATE DEHYDROGENASE (GDH) IN FECES - C. DIFFICILE - ANVISA Registration 81086830102

Access comprehensive regulatory information for GLUTAMATE DEHYDROGENASE (GDH) IN FECES - C. DIFFICILE in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81086830102 and manufactured by VEDALAB. The registration is held by FASTTEST DISTRIBUIDORA DE PRODUTOS PARA LABORATร“RIOS LTDA with validity until Mar 24, 2035.

This page provides complete technical specifications for 2 related devices, regulatory compliance details. 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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81086830102
2 Related Devices
Registration Details
ANVISA Registration Number: 81086830102
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Related Devices (2)

Registration Details

81086830102

25351354186202441

20037992000139

Company Information

VEDALAB
France
PT: FRANร‡A

Dates and Status

Mar 24, 2025

24/03/2035

09/18/2025 19:00:01

Registration Details

81086830102

25351354186202441

20037992000139

Dates and Status

Mar 24, 2025

24/03/2035

09/18/2025 19:00:01