Taiwan FDA registration cfd5fe4ed9701912ae86240dcb5d3c2e
"Daiei" grinding device and its accessories (unsterilized)
TW: "大榮" 研磨裝置及其附件 (未滅菌)
Registration details
- Analysis ID
- cfd5fe4ed9701912ae86240dcb5d3c2e
- Customs Code
- DHA084a0018601
Company information
- Manufacturer
- DAIEI DENTAL PRODUCTS Co., Ltd.
- Manufacturer Country
- Japan
- Authorized Representative
- POPLAR CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of grinding devices and their accessories (F.6010) of the classification and grading management methods for medical equipment.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.6010 Abrasive devices and accessories thereof
Dates and status
- Registration Date
- Jun 02, 2023
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Daiei" grinding device and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cfd5fe4ed9701912ae86240dcb5d3c2e and manufactured by DAIEI DENTAL PRODUCTS Co., Ltd.. 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.
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