Taiwan FDA registration 5e00159bb4b504e2bd9f33c6eaf7607d

CAPOSS Bone Graft Substitute

TW: 肯柏世人工骨填充物

Taiwan·Risk Class 2·MD·SHINEO TECHNOLOGY CO., LTD.·Registered Mar 07, 2016 – Mar 07, 2026Expired

Registration details

Analysis ID: 5e00159bb4b504e2bd9f33c6eaf7607d
License Form: Ministry of Health Medical Device Manufacturing No. 005272

Company information

Manufacturer: SHINEO TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHINEO TECHNOLOGY 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): N3045 Resorbed calcium salt bone cavity filling device
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 07, 2016
Expiry Date: Mar 07, 2026

About this record

Access comprehensive regulatory information for CAPOSS Bone Graft Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e00159bb4b504e2bd9f33c6eaf7607d and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..

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