Philippines FDA registration MDR-10097
DYONICS 4.0mm ELITE ACROMIOBLASTER BURR
Philippines·Smith & Nephew Pte. Ltd.·USA·Issued July 30, 2020 – July 30, 2021Device information
- Product Name
- DYONICS 4.0mm ELITE ACROMIOBLASTER BURR
- Registration Number
- MDR-10097
Manufacturer details
- Manufacturer
- Smith & Nephew Pte. Ltd.
- Country of Origin
- USA
Importer & distribution
- Importer/Distributor
- Endomed Trading, Inc.
Registration dates
- Issuance Date
- July 30, 2020
- Expiry Date
- July 30, 2021
About this record
Access comprehensive regulatory information for DYONICS 4.0mm ELITE ACROMIOBLASTER BURR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10097 and manufactured by Smith & Nephew Pte. Ltd. in USA. The device was registered on July 30, 2020.
This page provides complete registration details including manufacturer information, importer/distributor details (Endomed Trading, 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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