Taiwan FDA registration 167816154ad897b5ab4c4d25c4da510f
"Force Guidance" Dental Intraosseous Implant Attachment (Unsterilized)
TW: “力的導引”牙齒骨內植入物附件 (未滅菌)
Registration details
- Analysis ID
- 167816154ad897b5ab4c4d25c4da510f
Company information
- Manufacturer
- Guanghong Technology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LEADERGUIDE INTERNATIONAL CO., LTD.
Product details
- Intended Use
- Limited to the first-level identification scope of the Measures for the Administration of Medical Devices "Dental Implant Attachment (F.3980)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3980 Intradental implant manipulation equipment
- Import Information
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Mar 10, 2009
- Expiry Date
- Mar 10, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Force Guidance" Dental Intraosseous Implant Attachment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 167816154ad897b5ab4c4d25c4da510f and manufactured by Guanghong Technology Co., Ltd. The authorized representative in Taiwan is LEADERGUIDE INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices