Philippines FDA registration CMDR-2024-02451C

NuVasive VuePoint II OCT system - Keel Plate

Philippines·NuVasive, Inc. 7475 Lusk Blvd. San Diego, California 92121, USA·USA·Issued April 08, 2024 – March 20, 2029

Device information

Product Name: NuVasive VuePoint II OCT system - Keel Plate
Registration Number: CMDR-2024-02451C

Manufacturer details

Manufacturer: NuVasive, Inc. 7475 Lusk Blvd. San Diego, California 92121, USA
Country of Origin: USA

Importer & distribution

Importer/Distributor: PacificSurgical Inc.

Registration dates

Issuance Date: April 08, 2024
Expiry Date: March 20, 2029

About this record

Access comprehensive regulatory information for NuVasive VuePoint II OCT system - Keel Plate in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02451C and manufactured by NuVasive, Inc. 7475 Lusk Blvd. San Diego, California 92121, USA in USA. The device was registered on April 08, 2024.

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