Philippines FDA registration CMDR-2025-04739

Endopath® Xcel™ Dilating Tip Trocar with Stability Sleeve

Philippines flagPhilippines·Ethicon Endo-Surgery, LLC - 475 Calle C, Guaynabo, Puerto Rico 00969 USA Mfd. By: Nypro Precision Assembles (NPA) de Mexico S. De R.L. De C.V. - Blvd. Hector Teran Teran #20662-C, Col. Murua Oriente, Tijuana, 22465, Mexico·USA·Issued July 10, 2025 – July 10, 2030
Device information
Product Name
Endopath® Xcel™ Dilating Tip Trocar with Stability Sleeve
Registration Number
CMDR-2025-04739
Manufacturer details
Country of Origin
USA
Importer & distribution
Registration dates
Issuance Date
July 10, 2025
Expiry Date
July 10, 2030
About this record

Access comprehensive regulatory information for Endopath® Xcel™ Dilating Tip Trocar with Stability Sleeve in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04739 and manufactured by Ethicon Endo-Surgery, LLC - 475 Calle C, Guaynabo, Puerto Rico 00969 USA Mfd. By: Nypro Precision Assembles (NPA) de Mexico S. De R.L. De C.V. - Blvd. Hector Teran Teran #20662-C, Col. Murua Oriente, Tijuana, 22465, Mexico in USA. The device was registered on July 10, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Johnson & Johnson (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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