Philippines FDA registration DVR-5039

CURITY ORAL/NASAL TRACHEAL TUBE CUFFLESS MURPHY EYE

Name: CURITY ORAL/NASAL TRACHEAL TUBE CUFFLESS MURPHY EYE — Philippines FDA registration DVR-5039
Creator: Covidien Private Limited
Keywords: CURITY ORAL/NASAL TRACHEAL TUBE CUFFLESS MURPHY EYE, DVR-5039, Covidien Private Limited, Medtronic Philippines, Inc., USA, Philippines FDA registration

PhilippinesCovidien Private LimitedUSAIssued August 07, 2020 – April 15, 2025

VerifiedFDA Philippines · official registry

Device information

Product Name: CURITY ORAL/NASAL TRACHEAL TUBE CUFFLESS MURPHY EYE
Registration Number: DVR-5039

Manufacturer details

Manufacturer: Covidien Private Limited
Country of Origin: USA

Importer & distribution

Importer/Distributor: Medtronic Philippines, Inc.

Registration dates

Issuance Date: August 07, 2020
Expiry Date: April 15, 2025

About this record

Access comprehensive regulatory information for CURITY ORAL/NASAL TRACHEAL TUBE CUFFLESS MURPHY EYE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-5039 and manufactured by Covidien Private Limited in USA. The device was registered on August 07, 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.