Taiwan FDA registration 40e2d6883882ee7eb049edbc9a771396
"Ultradent" Halo Sectional Matrix System (Non-Sterile)
TW: "歐卓登特" 哈囉 成型牙隔固定套件組 (未滅菌)
Taiwan·Risk Class 1·MD·Ultradent Products, Inc.·Registered Jan 06, 2023 – Jan 06, 2028ActiveRegistration details
- Analysis ID
- 40e2d6883882ee7eb049edbc9a771396
- License Form
- Ministry of Health Medical Device Import No. 023004
- Customs Code
- DHA09402300408
Company information
- Manufacturer
- Ultradent Products, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- THONG TING TRADING COMPANY LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of dental hand instruments (F.4565).
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 06, 2023
- Expiry Date
- Jan 06, 2028
About this record
Access comprehensive regulatory information for "Ultradent" Halo Sectional Matrix System (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 40e2d6883882ee7eb049edbc9a771396 and manufactured by Ultradent Products, Inc.. The authorized representative in Taiwan is THONG TING TRADING COMPANY 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