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ATELLICA CH AMPHETAMINES (AMP) - FDA Registration IVDR-00440

Access comprehensive regulatory information for ATELLICA CH AMPHETAMINES (AMP) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00440 and manufactured by Siemens Healthcare GmbH Munich, Germany Mfd. By: Siemens Healthcare Diagnostics Inc. - MA, USA for Siemens Healthcare Diagnostics Inc. - NY, USA in Germany. The device was registered on January 20, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Siemens Healthcare Inc.), 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
IVDR-00440
ATELLICA CH AMPHETAMINES (AMP)
Registered medical device in Philippines
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Device Information
Product Name
ATELLICA CH AMPHETAMINES (AMP)
Registration Number
IVDR-00440
Importer & Distribution
Importer/Distributor
Siemens Healthcare Inc.
Registration Dates
Issuance Date
January 20, 2023
Expiry Date
November 21, 2025