Taiwan FDA registration 41d4e4351628c19391ad9547edcdf53f
"Swann Morton" Dental Hand Instrument (Non-Sterile)
TW: "史旺摩頓" 牙科手用器械 (未滅菌)
Registration details
- Analysis ID
- 41d4e4351628c19391ad9547edcdf53f
- License Form
- Ministry of Health Medical Device Import No. 015771
- Customs Code
- DHA09401577103
Company information
- Manufacturer
- SWANN - MORTON LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Sanye Limited
Product details
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F4565 Hand instruments for dental use
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 26, 2015
- Expiry Date
- Oct 26, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Swann Morton" Dental Hand Instrument (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 41d4e4351628c19391ad9547edcdf53f and manufactured by SWANN - MORTON LIMITED. The authorized representative in Taiwan is Sanye Limited.
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