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Relyx™ U200 Self Adhesive Resin Cement - FDA Registration MDR-00522

Access comprehensive regulatory information for Relyx™ U200 Self Adhesive Resin Cement in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-00522 and manufactured by 3M Deutschland GmbH- Carl-Schurz-Straße 1- 41453 Neuss Germany Mfd by: 3M Deustschland GmbH- ESPE Platz, 82229 Seefeld, Germany in Germany. The device was registered on March 19, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Alphadent 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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Germany
MDR-00522
Relyx™ U200 Self Adhesive Resin Cement
Registered medical device in Philippines
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Device Information
Product Name
Relyx™ U200 Self Adhesive Resin Cement
Registration Number
MDR-00522
Importer & Distribution
Importer/Distributor
Alphadent Corporation
Registration Dates
Issuance Date
March 19, 2025
Expiry Date
April 13, 2029