Philippines FDA registration MDR-09654

BD MAX™ UVE SPECIMEN COLLECTION KIT

Philippines·Becton Dickinson Holdings Pte. Ltd.·USA·Issued May 13, 2020 – May 13, 2021

Device information

Product Name: BD MAX™ UVE SPECIMEN COLLECTION KIT
Registration Number: MDR-09654

Manufacturer details

Manufacturer: Becton Dickinson Holdings Pte. Ltd.
Country of Origin: USA

Importer & distribution

Importer/Distributor: Patient Care Corporation

Registration dates

Issuance Date: May 13, 2020
Expiry Date: May 13, 2021

About this record

Access comprehensive regulatory information for BD MAX™ UVE SPECIMEN COLLECTION KIT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09654 and manufactured by Becton Dickinson Holdings Pte. Ltd. in USA. The device was registered on May 13, 2020.

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