Taiwan FDA registration 9c38bfabc57719755c549ca3aab09e7e
"Kenedict" Fixing Molds & Accessories (Indepleted)
TW: "肯尼帝克" 固定用模材及配件 (未滅菌)
Taiwan·Risk Class 1·KINETEC SAS·Registered Aug 12, 2024 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 9c38bfabc57719755c549ca3aab09e7e
- Customs Code
- DHA084A0029809
Company information
- Manufacturer
- KINETEC SAS
- Manufacturer Country
- France
- Authorized Representative
- BLESSING CATHAY CORPORATION
Product details
- Intended Use
- It is limited to the first level of identification of the classification and grading management of medical devices "splints for non-inflatable limbs (I.3910)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.3910 Clip board for non-bulging limbs
- Import Information
- import
Dates and status
- Registration Date
- Aug 12, 2024
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Kenedict" Fixing Molds & Accessories (Indepleted) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c38bfabc57719755c549ca3aab09e7e and manufactured by KINETEC SAS. The authorized representative in Taiwan is BLESSING CATHAY CORPORATION.
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