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REBORN ESSENCE LUMBAR FIXATION SYSTEM - SMOOTH ROD - FDA Registration MDR-08072I

Access comprehensive regulatory information for REBORN ESSENCE LUMBAR FIXATION SYSTEM - SMOOTH ROD in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-08072I and manufactured by Baui Biotech Co. Ltd. - New Taipei City, Taiwan R.O.C. in China. The device was registered on June 04, 2021.

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

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MDR-08072I
REBORN ESSENCE LUMBAR FIXATION SYSTEM - SMOOTH ROD
Registered medical device in Philippines
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Device Information
Product Name
REBORN ESSENCE LUMBAR FIXATION SYSTEM - SMOOTH ROD
Registration Number
MDR-08072I
Manufacturer Details
Importer & Distribution
Importer/Distributor
EG Healthcare, Inc.
Registration Dates
Issuance Date
June 04, 2021
Expiry Date
May 03, 2025