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Neodent NGS Mucosa Punch - FDA Registration CMDR-2025-04998

Access comprehensive regulatory information for Neodent NGS Mucosa Punch in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04998 and manufactured by Institut Straumann AG - Peter Merian - Weg 12, 4002, Basel, Switzerland Mfd. By: JJGC Industria e Comercio de Materials Dentarios SA - Avenida Juscelino Kubitschek de Oliveira, 3291 - Curitiba-PR, Brasil in Switzerland. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Metro DNC Marketing Corporation), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

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Switzerland
CMDR-2025-04998
Neodent NGS Mucosa Punch
Registered medical device in Philippines
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Device Information
Product Name
Neodent NGS Mucosa Punch
Registration Number
CMDR-2025-04998
Importer & Distribution
Registration Dates
Issuance Date
July 10, 2025
Expiry Date
July 10, 2030