Philippines FDA registration MDR-01843

UROMAX ULTRA™ BALLOON DILATATION CATHETER

Name: UROMAX ULTRA™ BALLOON DILATATION CATHETER — Philippines FDA registration MDR-01843
Creator: Boston Scientific Corporation
Keywords: UROMAX ULTRA™ BALLOON DILATATION CATHETER, MDR-01843, Boston Scientific Corporation, Boston Scientific Phils., Inc., Ireland, Philippines FDA registration

PhilippinesBoston Scientific CorporationIrelandIssued March 18, 2020 – February 25, 2025

VerifiedFDA Philippines · official registry

Device information

Product Name: UROMAX ULTRA™ BALLOON DILATATION CATHETER
Registration Number: MDR-01843

Manufacturer details

Manufacturer: Boston Scientific Corporation
Country of Origin: Ireland

Importer & distribution

Importer/Distributor: Boston Scientific Phils., Inc.

Registration dates

Issuance Date: March 18, 2020
Expiry Date: February 25, 2025

About this record

Access comprehensive regulatory information for UROMAX ULTRA™ BALLOON DILATATION CATHETER in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01843 and manufactured by Boston Scientific Corporation in Ireland. The device was registered on March 18, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Boston Scientific Phils., 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.