Taiwan FDA registration 1a76848e0cf49578208a4c14a04cbb7a
“Vertex”Base plate shellac (non-sterile)
TW: “陀帝士”基底塗料 (未滅菌)
Registration details
- Analysis ID
- 1a76848e0cf49578208a4c14a04cbb7a
- License Form
- Ministry of Health Medical Device Import No. 022308
- Customs Code
- DHA09402230800
Company information
- Manufacturer
- VERTEX-DENTAL B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- POPLAR CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of base coatings (F.6200) of the medical equipment management measures.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F6200 base coating
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 17, 2021
- Expiry Date
- Feb 17, 2026
About this record
Access comprehensive regulatory information for “Vertex”Base plate shellac (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 1a76848e0cf49578208a4c14a04cbb7a and manufactured by VERTEX-DENTAL B.V.. The authorized representative in Taiwan is POPLAR CO., LTD..
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