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Karl Storz Flex. Intubat. Videoendoscope 5.5x66, Set - FDA Registration CMDR-2025-03815

Access comprehensive regulatory information for Karl Storz Flex. Intubat. Videoendoscope 5.5x66, Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-03815 and manufactured by Karl Storz SE & Co. KG in Germany. The device was registered on February 04, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Karl Storz Endoscopy 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-2025-03815
Karl Storz Flex. Intubat. Videoendoscope 5.5x66, Set
Registered medical device in Philippines
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Device Information
Product Name
Karl Storz Flex. Intubat. Videoendoscope 5.5x66, Set
Registration Number
CMDR-2025-03815
Manufacturer Details
Country of Origin
Germany
Importer & Distribution
Registration Dates
Issuance Date
February 04, 2025
Expiry Date
February 04, 2030