Taiwan FDA registration 98cc1b7036ef9ff2f400c8f41102302d
Anchor Tec grinding device and its accessories (unsterilized)
TW: “安克典特”研磨裝置及其附件（未滅菌）
Taiwan·Risk Class 1·MK-DENT GMBH·Registered Nov 22, 2010 – Nov 22, 2025CancelledRegistration details
- Analysis ID
- 98cc1b7036ef9ff2f400c8f41102302d
- Customs Code
- DHA04400954900
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 Dentistry
- Product Type (Level 2)
- F.6010 Abrasive devices and accessories thereof
- Import Information
- import
Dates and status
- Registration Date
- Nov 22, 2010
- Expiry Date
- Nov 22, 2025
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Anchor Tec grinding device and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 98cc1b7036ef9ff2f400c8f41102302d and manufactured by MK-DENT GMBH. The authorized representative in Taiwan is LI-XIANG INTERNATIONAL CO., LTD..
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