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VERSAONE™ FASCIAL CLOSURE SYSTEM, BLADED TROCAR WITH FIXATION CANNULA, 12mm STANDARD - FDA Registration MDR-10056A

Access comprehensive regulatory information for VERSAONE™ FASCIAL CLOSURE SYSTEM, BLADED TROCAR WITH FIXATION CANNULA, 12mm STANDARD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10056A and manufactured by Covidien Private Limited in USA. The device was registered on July 23, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronic 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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USA
MDR-10056A
VERSAONE™ FASCIAL CLOSURE SYSTEM, BLADED TROCAR WITH FIXATION CANNULA, 12mm STANDARD
Registered medical device in Philippines
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Device Information
Product Name
VERSAONE™ FASCIAL CLOSURE SYSTEM, BLADED TROCAR WITH FIXATION CANNULA, 12mm STANDARD
Registration Number
MDR-10056A
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Medtronic Philippines, Inc.
Registration Dates
Issuance Date
July 23, 2020
Expiry Date
July 23, 2021