Philippines FDA registration DVR-2370

PORTEX TUOHY NEEDLE

Name: PORTEX TUOHY NEEDLE — Philippines FDA registration DVR-2370
Creator: Smiths Medical International Ltd.
Keywords: PORTEX TUOHY NEEDLE, DVR-2370, Smiths Medical International Ltd., Rebmann Inc., Mexico, Philippines FDA registration

PhilippinesSmiths Medical International Ltd.MexicoIssued January 22, 2019 – August 14, 2023

VerifiedFDA Philippines · official registry

Device information

Product Name: PORTEX TUOHY NEEDLE
Registration Number: DVR-2370

Manufacturer details

Manufacturer: Smiths Medical International Ltd.
Country of Origin: Mexico

Importer & distribution

Importer/Distributor: Rebmann Inc.

Registration dates

Issuance Date: January 22, 2019
Expiry Date: August 14, 2023

About this record

Access comprehensive regulatory information for PORTEX TUOHY NEEDLE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-2370 and manufactured by Smiths Medical International Ltd. in Mexico. The device was registered on January 22, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Rebmann 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.