Taiwan FDA registration 7b2c3286598f6a3287ada9cb0ad07a90
“MK-dent”Abrasive Devices and Accessories (Non-Sterile)
TW: “安克典特”研磨裝置及其附件（未滅菌）
Taiwan·Risk Class 1·MD·MK-DENT GMBH·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- 7b2c3286598f6a3287ada9cb0ad07a90
- License Form
- Ministry of Health Medical Device Import Registration No. 009549
- Customs Code
- DHA08400954907
Company information
- Manufacturer
- MK-DENT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- LI-XIANG INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) under the management measures for medical equipment.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for “MK-dent”Abrasive Devices 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 7b2c3286598f6a3287ada9cb0ad07a90 and manufactured by MK-DENT GMBH. The authorized representative in Taiwan is LI-XIANG INTERNATIONAL CO., LTD..
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