Myanmar FDA registration 900ef72abb67068043e267afe0bfe8b9

Percuflex TM Ureteral Stent

Name: Percuflex TM Ureteral Stent — Myanmar FDA registration 900ef72abb67068043e267afe0bfe8b9
Creator: Boston Scientific Corporation
Keywords: Percuflex TM Ureteral Stent, Percuflex TM Ureteral Stent, Boston Scientific, 900ef72abb67068043e267afe0bfe8b9, Myanmar FDA registration

MyanmarBoston ScientificBoston Scientific CorporationRegistered August 05, 2022

VerifiedFDA Myanmar · official registry

Device classification

Brand Name: Boston Scientific

Registration information

Analysis ID: 900ef72abb67068043e267afe0bfe8b9
Registration Date: August 05, 2022

Manufacturer

Name: Boston Scientific Corporation

Authorized Representative

Name: CONCORDIA INTERNATIONAL COMPANY LIMITED

About this record

Access comprehensive regulatory information for Percuflex TM Ureteral Stent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 900ef72abb67068043e267afe0bfe8b9 and manufactured by Boston Scientific Corporation. The device was registered on August 05, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.