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CINtec PLUS Cytology Kit - FDA Registration dd383bbf2c298b01f5f5ce0e25a7cbac

Access comprehensive regulatory information for CINtec PLUS Cytology Kit in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dd383bbf2c298b01f5f5ce0e25a7cbac and manufactured by Ventana Medical Systems, Inc.. The device was registered on August 02, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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dd383bbf2c298b01f5f5ce0e25a7cbac
CINtec PLUS Cytology Kit
FDA ID: dd383bbf2c298b01f5f5ce0e25a7cbac
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Device Classification
Brand Name
ROCHE Brand
Registration Information
Analysis ID
dd383bbf2c298b01f5f5ce0e25a7cbac
Registration Date
August 02, 2022
Authorized Representative