Taiwan FDA registration 7f5a711d0b59f12dc45e3cad9e318724

ReBorn Essence Canis Lumbar Intervertebral Cage

TW: “瑞寶億”肯尼斯腰椎椎間融合器

Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Feb 05, 2021 – Feb 05, 2026Expired

Registration details

Analysis ID: 7f5a711d0b59f12dc45e3cad9e318724
License Form: Ministry of Health Medical Device Manufacturing No. 007067

Company information

Manufacturer: BAUI BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BAUI BIOTECH CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N3080 Interbody fusion device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Feb 05, 2021
Expiry Date: Feb 05, 2026

About this record

Access comprehensive regulatory information for ReBorn Essence Canis Lumbar Intervertebral Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f5a711d0b59f12dc45e3cad9e318724 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

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