Philippines FDA registration MDR-09833A

STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET

Name: STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET — Philippines FDA registration MDR-09833A
Creator: Transmedic Pte. Ltd.
Keywords: STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET, MDR-09833A, Transmedic Pte. Ltd., Transmedic Philippines, Inc., Germany, Philippines FDA registration

PhilippinesTransmedic Pte. Ltd.GermanyIssued April 20, 2022 – June 29, 2026

VerifiedFDA Philippines · official registry

Device information

Product Name: STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET
Registration Number: MDR-09833A

Manufacturer details

Manufacturer: Transmedic Pte. Ltd.
Country of Origin: Germany

Importer & distribution

Importer/Distributor: Transmedic Philippines, Inc.

Registration dates

Issuance Date: April 20, 2022
Expiry Date: June 29, 2026

About this record

Access comprehensive regulatory information for STRYKER® PNEUMOCLEAR™ HIGH-FLOW TUBE SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09833A and manufactured by Transmedic Pte. Ltd. in Germany. The device was registered on April 20, 2022.

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