Taiwan FDA registration a7d2f7b050d1b60505232e40c86d0f17

“MDBT” Peri. & Implant Screw (Non-Sterile)

TW: “民德生醫”骨內植入加強釘(未滅菌)

Taiwan·Risk Class 2·MD·M.D.B.T. CO., LTD.·Registered Aug 04, 2013 – Aug 04, 2028Active

Registration details

Analysis ID: a7d2f7b050d1b60505232e40c86d0f17
License Form: Ministry of Health Medical Device Manufacturing No. 004211

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: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): F Dental devices
Product Type (Level 2): F4880 Intraosseous fixing screws or metal wires
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 04, 2013
Expiry Date: Aug 04, 2028

About this record

Access comprehensive regulatory information for “MDBT” Peri. & Implant Screw (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a7d2f7b050d1b60505232e40c86d0f17 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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