Philippines FDA registration DVR-8767

Ruschelit® Safety Clear Plus Tracheal Tube

Name: Ruschelit® Safety Clear Plus Tracheal Tube — Philippines FDA registration DVR-8767
Creator: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, Malaysia
Keywords: Ruschelit® Safety Clear Plus Tracheal Tube, DVR-8767, Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, Malaysia, East Lane Corporation, Ireland, Philippines FDA registration

PhilippinesTeleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, MalaysiaIrelandIssued May 09, 2024 – February 28, 2029

VerifiedFDA Philippines · official registry

Device information

Product Name: Ruschelit® Safety Clear Plus Tracheal Tube
Registration Number: DVR-8767

Manufacturer details

Manufacturer: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, Malaysia
Country of Origin: Ireland

Importer & distribution

Importer/Distributor: East Lane Corporation

Registration dates

Issuance Date: May 09, 2024
Expiry Date: February 28, 2029

About this record

Access comprehensive regulatory information for Ruschelit® Safety Clear Plus Tracheal Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-8767 and manufactured by Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone Co. Westmeath, Ireland Mfd By: Teleflex Medical-IDA Business and Technology Park, Dublin Road, Athlone, Co. Westmeath, Ireland Mfd By: Teleflex Cor. Roosevelt Sdn-Kamunting Perak, Malaysia in Ireland. The device was registered on May 09, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (East Lane Corporation), 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.