Taiwan FDA registration 50f494d726ab522166548d4c1552d98f
"Vericom" Surgical Guide (Non-Sterile)
TW: "葳爾康" 手術導板 (未滅菌)
Taiwan·Risk Class 1·MD·VERICOM CO., LTD.·Registered Sep 28, 2020 – Sep 28, 2025ExpiredRegistration details
- Analysis ID
- 50f494d726ab522166548d4c1552d98f
- License Form
- Ministry of Health Medical Device Import No. 021999
- Customs Code
- DHA09402199906
Company information
- Manufacturer
- VERICOM CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SUNDENT CORPORATION
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 Dental devices
- Product Type (Level 2)
- F3980 Dental Intraosseous Implant Attachment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 28, 2020
- Expiry Date
- Sep 28, 2025
About this record
Access comprehensive regulatory information for "Vericom" Surgical Guide (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 50f494d726ab522166548d4c1552d98f and manufactured by VERICOM CO., LTD.. The authorized representative in Taiwan is SUNDENT CORPORATION.
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