Taiwan FDA registration a1ebe2eef4c65163571e87fc2f285d14
“GC”Occlusal analysis device & accessories (Non-Sterile)
TW: “而至”牙科咬合分析裝置及其附件 (未滅菌)
Registration details
- Analysis ID
- a1ebe2eef4c65163571e87fc2f285d14
- License Form
- Ministry of Health Medical Device Import No. 019944
- Customs Code
- DHA09401994402
Company information
- Manufacturer
- GC CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- GC TAIWAN DENTAL CORPORATION
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6140 Occlusal paper
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 21, 2018
- Expiry Date
- Dec 21, 2023
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for “GC”Occlusal analysis device & 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 a1ebe2eef4c65163571e87fc2f285d14 and manufactured by GC CORPORATION. The authorized representative in Taiwan is GC TAIWAN DENTAL CORPORATION.
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.
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