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BoneScalpel Blade - FDA Registration CMDR-2025-03771

Access comprehensive regulatory information for BoneScalpel Blade in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03771 and manufactured by Misonix, Inc. in USA. The device was registered on January 31, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Pacific Surgical, 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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USA
CMDR-2025-03771
BoneScalpel Blade
Registered medical device in Philippines
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Device Information
Product Name
BoneScalpel Blade
Registration Number
CMDR-2025-03771
Manufacturer Details
Manufacturer
Misonix, Inc.
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Pacific Surgical, Inc.
Registration Dates
Issuance Date
January 31, 2025
Expiry Date
January 31, 2030