Taiwan FDA registration 22203872f5887643bebe237de25bff0a
"Parkell" Retraction Paste (Non-Sterile)
TW: "派克" 排齦膏 (未滅菌)
Taiwan·Risk Class 1·MD·PARKELL, INC.·Registered Aug 08, 2018 – Aug 08, 2028ActiveRegistration details
- Analysis ID
- 22203872f5887643bebe237de25bff0a
- License Form
- Ministry of Health Medical Device Import No. 019467
- Customs Code
- DHA09401946707
Company information
- Manufacturer
- PARKELL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- FRANKFURT TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the gingival line (F.0001) of the medical equipment management method.
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F0001 Gingival drain line
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 08, 2018
- Expiry Date
- Aug 08, 2028
About this record
Access comprehensive regulatory information for "Parkell" Retraction Paste (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 22203872f5887643bebe237de25bff0a and manufactured by PARKELL, INC.. The authorized representative in Taiwan is FRANKFURT TECHNOLOGY 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