Philippines FDA registration MDR-09859B

BIOMET INTERLOK FIXED I-BEAM TIBIAL TRAY PLATE WITH LOCKING BAR

Philippines·Zimmer Pte. Ltd.·USA·Issued July 02, 2020 – July 02, 2021

Device information

Product Name: BIOMET INTERLOK FIXED I-BEAM TIBIAL TRAY PLATE WITH LOCKING BAR
Registration Number: MDR-09859B

Manufacturer details

Manufacturer: Zimmer Pte. Ltd.
Country of Origin: USA

Importer & distribution

Importer/Distributor: Asia Actual Consultancy Inc.

Registration dates

Issuance Date: July 02, 2020
Expiry Date: July 02, 2021

About this record

Access comprehensive regulatory information for BIOMET INTERLOK FIXED I-BEAM TIBIAL TRAY PLATE WITH LOCKING BAR in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-09859B and manufactured by Zimmer Pte. Ltd. in USA. The device was registered on July 02, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Asia Actual Consultancy 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.