Philippines FDA registration MDR-10022F

REBORN ESSENCE POSTERIOR CERVICAL PLATE SYSTEM - CERVICAL ROD HOOK - NON-STERILE

Philippines flagPhilippines·BAUI Biotech Co., Ltd.·Taiwan·Issued July 15, 2020 – July 15, 2021
Device information
Product Name
REBORN ESSENCE POSTERIOR CERVICAL PLATE SYSTEM - CERVICAL ROD HOOK - NON-STERILE
Registration Number
MDR-10022F
Manufacturer details
Country of Origin
Taiwan
Importer & distribution
Importer/Distributor
EG Healthcare Inc.
Registration dates
Issuance Date
July 15, 2020
Expiry Date
July 15, 2021
About this record

Access comprehensive regulatory information for REBORN ESSENCE POSTERIOR CERVICAL PLATE SYSTEM - CERVICAL ROD HOOK - NON-STERILE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10022F and manufactured by BAUI Biotech Co., Ltd. in Taiwan. The device was registered on July 15, 2020.

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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