Taiwan FDA registration aa5d43a4534c31a3801d84cbd7613c43
"Gower" dental tungsten carbide round head file (unsterilized)
TW: “高爾”牙科用碳化鎢圓頭銼 (未滅菌)
Taiwan·Risk Class 1·KERR - BEAVERS DENTAL DIVISION·Registered Jul 22, 2009 – Jul 22, 2024ExpiredRegistration details
- Analysis ID
- aa5d43a4534c31a3801d84cbd7613c43
- Customs Code
- DHA04400793100
Company information
- Manufacturer
- KERR - BEAVERS DENTAL DIVISION
- Manufacturer Country
- Canada
- Authorized Representative
- TE CHANG MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, dental drill needle (F.3240) first level identification range.
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3240 Dental drill pins
- Import Information
- import
Dates and status
- Registration Date
- Jul 22, 2009
- Expiry Date
- Jul 22, 2024
About this record
Access comprehensive regulatory information for "Gower" dental tungsten carbide round head file (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aa5d43a4534c31a3801d84cbd7613c43 and manufactured by KERR - BEAVERS DENTAL DIVISION. The authorized representative in Taiwan is TE CHANG MEDICAL INSTRUMENT 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