Taiwan FDA registration 355364dfb67425380cbca2464cbab9d3

"Wieland" abrasive device and accessories (Non-Sterile)

TW: "維爾蘭" 研磨裝置及其附件(未滅菌)

Taiwan·Risk Class 1·MD·WIELAND DENTAL + TECHNIK GMBH & CO. KG·Registered Mar 11, 2016 – Mar 11, 2021Cancelled

Registration details

Analysis ID: 355364dfb67425380cbca2464cbab9d3
License Form: Ministry of Health Medical Device Import No. 016246
Customs Code: DHA09401624602

Company information

Manufacturer: WIELAND DENTAL + TECHNIK GMBH & CO. KG
Manufacturer Country: Germany
Authorized Representative: MYWAY INTERNATIONAL CO., LTD.

Product details

Product Type (Level 1): F Dental devices
Product Type (Level 2): F6010 Grinding device and accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 11, 2016
Expiry Date: Mar 11, 2021
Cancellation Date: Feb 06, 2020

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Wieland" abrasive device and accessories (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 355364dfb67425380cbca2464cbab9d3 and manufactured by WIELAND DENTAL + TECHNIK GMBH & CO. KG. The authorized representative in Taiwan is MYWAY INTERNATIONAL CO., LTD..

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