Philippines FDA registration CMDR-2025-04959

Stryker® Fluted Drum

Name: Stryker® Fluted Drum — Philippines FDA registration CMDR-2025-04959
Creator: Transmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd. - Instruments Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork, T45 HV12, Ireland For: Stryker Instruments - 1941 Stryker Way, Portage, MI 49002, USA
Keywords: Stryker® Fluted Drum, CMDR-2025-04959, Transmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd. - Instruments Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork, T45 HV12, Ireland For: Stryker Instruments - 1941 Stryker Way, Portage, MI 49002, USA, Transmedic Philippines, Inc., Singapore, Philippines FDA registration

PhilippinesTransmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd. - Instruments Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork, T45 HV12, Ireland For: Stryker Instruments - 1941 Stryker Way, Portage, MI 49002, USASingaporeIssued July 10, 2025 – July 10, 2030

VerifiedFDA Philippines · official registry

Device information

Product Name: Stryker® Fluted Drum
Registration Number: CMDR-2025-04959

Manufacturer details

Manufacturer: Transmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd. - Instruments Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork, T45 HV12, Ireland For: Stryker Instruments - 1941 Stryker Way, Portage, MI 49002, USA
Country of Origin: Singapore

Importer & distribution

Importer/Distributor: Transmedic Philippines, Inc.

Registration dates

Issuance Date: July 10, 2025
Expiry Date: July 10, 2030

About this record

Access comprehensive regulatory information for Stryker® Fluted Drum in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04959 and manufactured by Transmedic Pte Ltd - 5 Jalan Kilang Barat, 9th Floor Petro Centre, Singapore 159349 Mfd. By: Stryker Ireland Ltd. - Instruments Division - Carrigtwohill Business & Technology Park, Carrigtwohill, Co Cork, T45 HV12, Ireland For: Stryker Instruments - 1941 Stryker Way, Portage, MI 49002, USA in Singapore. The device was registered on July 10, 2025.

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.