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PreciTotal PreciTotal Knee System - Stemmed Polished - FDA Registration CMDR-2023-01374D

Access comprehensive regulatory information for PreciTotal PreciTotal Knee System - Stemmed Polished in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2023-01374D and manufactured by AAP Joints GmbH Wilhelm-von-Siemens-Str. 23, Aufgang F, 12277 Berlin, Germany Mfd By: Youshi Medical Suzhou Co., Ltd. - 1&2F Building 2 South No. 188 Jianglingjiang, Suzhou City, Jiangsu Province, 215163, P.R. China in Germany. The device was registered on March 14, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Somnotec Philippines, 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
CMDR-2023-01374D
PreciTotal PreciTotal Knee System - Stemmed Polished
Registered medical device in Philippines
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Device Information
Product Name
PreciTotal PreciTotal Knee System - Stemmed Polished
Registration Number
CMDR-2023-01374D
Importer & Distribution
Importer/Distributor
Somnotec Philippines, Inc.
Registration Dates
Issuance Date
March 14, 2023
Expiry Date
March 14, 2028