Taiwan FDA registration c21335b3cc7985a7be41c6f19e51c331
“Rainbow” Porcelain
TW: “瑞玻” 瓷粉
Taiwan·Risk Class 2·MD·Genoss Co., Ltd.·Registered Mar 28, 2018 – Mar 28, 2023ExpiredRegistration details
- Analysis ID
- c21335b3cc7985a7be41c6f19e51c331
- License Form
- Ministry of Health Medical Device Import No. 031003
- Customs Code
- DHA05603100308
Company information
- Manufacturer
- Genoss Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- MRS MICRO-WORK COMPANY LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6660 Dental porcelain powder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 28, 2018
- Expiry Date
- Mar 28, 2023
About this record
Access comprehensive regulatory information for “Rainbow” Porcelain in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c21335b3cc7985a7be41c6f19e51c331 and manufactured by Genoss Co., Ltd.. The authorized representative in Taiwan is MRS MICRO-WORK COMPANY LIMITED.
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