Taiwan FDA registration ddb64d1d212af5263e32820d17a8e338

“Ti-plus” Orthopedic manual surgical instruments (Non-sterile)

TW: “鈦嘉”手動式骨科手術器械(未滅菌)

Taiwan·Risk Class 1·MD·Ytterbium Technology Co., Ltd. head office·Registered Mar 05, 2019 – Mar 05, 2024Expired

Registration details

Analysis ID: ddb64d1d212af5263e32820d17a8e338
License Form: Ministry of Health Medical Device Manufacturing No. 007667

Company information

Manufacturer: Ytterbium Technology Co., Ltd. head office
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Ytterbium Technology Co., Ltd. head office

Product details

Intended Use: Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N4540 Manual osteologic surgery instrument
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Mar 05, 2019
Expiry Date: Mar 05, 2024

About this record

Access comprehensive regulatory information for “Ti-plus” Orthopedic manual surgical instruments (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ddb64d1d212af5263e32820d17a8e338 and manufactured by Ytterbium Technology Co., Ltd. head office. The authorized representative in Taiwan is Ytterbium Technology Co., Ltd. head office.

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