Pure Global

KARL STORZ Uretero-REno-Fiberscope FLEX-X2S, Set - FDA Registration CMDR-2025-04698

Access comprehensive regulatory information for KARL STORZ Uretero-REno-Fiberscope FLEX-X2S, Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04698 and manufactured by KARL STORZ SE & Co. KG - Dr.-Karl-Storz-StraรŸe 34 78532 Tuttlingen Germany Mfd. By: KARL STORZ Endovision, Inc. - 91 Carpenter Hill Road, Charlton MA 01507, USA in Germany. The device was registered on June 17, 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.

Free Database
Powered by Pure Global AI
FDA Official Data
Germany
CMDR-2025-04698
KARL STORZ Uretero-REno-Fiberscope FLEX-X2S, Set
Registered medical device in Philippines
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Information
Product Name
KARL STORZ Uretero-REno-Fiberscope FLEX-X2S, Set
Registration Number
CMDR-2025-04698
Importer & Distribution
Registration Dates
Issuance Date
June 17, 2025
Expiry Date
June 17, 2030