Taiwan FDA registration ce0f4fafdc351a8290091d236bbae38a
“SHOFU” DISK ZR Lucent Supra
TW: “松風”路森蘇培拉氧化鋯瓷盤
Taiwan·Risk Class 2·MD·Akita Adamant Co., Ltd.·Registered Apr 12, 2022 – Apr 12, 2027ActiveRegistration details
- Analysis ID
- ce0f4fafdc351a8290091d236bbae38a
- License Form
- Ministry of Health Medical Device Import No. 035377
- Customs Code
- DHA05603537704
Company information
- Manufacturer
- Akita Adamant Co., Ltd.
- Manufacturer Country
- Japan
- Authorized Representative
- SHOFU INC., TAIWAN BRANCH (JAPAN)
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F6660 Dental porcelain powder
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 12, 2022
- Expiry Date
- Apr 12, 2027
About this record
Access comprehensive regulatory information for “SHOFU” DISK ZR Lucent Supra in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce0f4fafdc351a8290091d236bbae38a and manufactured by Akita Adamant Co., Ltd.. The authorized representative in Taiwan is SHOFU INC., TAIWAN BRANCH (JAPAN).
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