Taiwan FDA registration 7eb54a2c537c71306f891e271ba52988
“Willmann & Pein” Competence Universal Light-Curing Universal Hybrid Composite
TW: “威爾麥潘”通用光固化複合樹脂
Taiwan·Risk Class 2·MD·WILLMANN & PEIN GMBH·Registered Aug 31, 2019 – Aug 31, 2024ExpiredRegistration details
- Analysis ID
- 7eb54a2c537c71306f891e271ba52988
- License Form
- Ministry of Health Medical Device Import No. 032825
- Customs Code
- DHA05603282503
Company information
- Manufacturer
- WILLMANN & PEIN GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDICAL SOLUTION INTERNATIONAL CO., LTD
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)
- F3690 Resin tusk wood
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 31, 2019
- Expiry Date
- Aug 31, 2024
About this record
Access comprehensive regulatory information for “Willmann & Pein” Competence Universal Light-Curing Universal Hybrid Composite in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7eb54a2c537c71306f891e271ba52988 and manufactured by WILLMANN & PEIN GMBH. The authorized representative in Taiwan is MEDICAL SOLUTION INTERNATIONAL CO., LTD.
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