Taiwan FDA registration 93e78f1b88714818599af37fe97c4305
"Dunshpie" Deremalay Rubber Needle (Unsterilized)
TW: “登士派”德瑞馬來膠針 (未滅菌)
Taiwan·Risk Class 1·DENTSPLY DENTAL (TIANJIN) CO., LTD.·Registered Jul 23, 2008 – Jul 23, 2018CancelledRegistration details
- Analysis ID
- 93e78f1b88714818599af37fe97c4305
- Customs Code
- DHA04600054002
Company information
- Manufacturer
- DENTSPLY DENTAL (TIANJIN) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Taiwan Branch of American Denspie Co., Ltd
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Malay Rubber (F.3850)".
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3850 Malay gum
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jul 23, 2008
- Expiry Date
- Jul 23, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Dunshpie" Deremalay Rubber Needle (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93e78f1b88714818599af37fe97c4305 and manufactured by DENTSPLY DENTAL (TIANJIN) CO., LTD.. The authorized representative in Taiwan is Taiwan Branch of American Denspie 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