Taiwan FDA registration 30030a558f00008e1cb114b7a67ded52

"MDBT" Orthopedic manual surgical instrument (Non-Sterile)

TW: "民德生醫" 手動式骨科手術器械 (未滅菌)

Taiwan·Risk Class 1·MD·M.D.B.T. CO., LTD.·Registered Jun 23, 2017 – Jun 23, 2022Expired

Registration details

Analysis ID: 30030a558f00008e1cb114b7a67ded52
License Form: Ministry of Health Medical Device Manufacturing No. 006800

Company information

Manufacturer: M.D.B.T. CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: M.D.B.T. CO., LTD.

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: Jun 23, 2017
Expiry Date: Jun 23, 2022

About this record

Access comprehensive regulatory information for "MDBT" Orthopedic manual surgical instrument (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 30030a558f00008e1cb114b7a67ded52 and manufactured by M.D.B.T. CO., LTD.. The authorized representative in Taiwan is M.D.B.T. CO., LTD..

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