Taiwan FDA registration a65492b09e4e013f55a63258dbea8ba7
"Syntellix" Orthopedic manual surgical instrument (Non-Sterile)
TW: "信德立" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·Syntellix AG·Registered Jul 03, 2020 – Jul 03, 2025ExpiredRegistration details
- Analysis ID
- a65492b09e4e013f55a63258dbea8ba7
- License Form
- Ministry of Health Medical Device Import No. 021696
- Customs Code
- DHA09402169601
Company information
- Manufacturer
- Syntellix AG
- Manufacturer Country
- Germany
- Authorized Representative
- MEDLION BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of manual orthopedic surgical instruments (N.4540) of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 03, 2020
- Expiry Date
- Jul 03, 2025
About this record
Access comprehensive regulatory information for "Syntellix" Orthopedic manual surgical 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 a65492b09e4e013f55a63258dbea8ba7 and manufactured by Syntellix AG. The authorized representative in Taiwan is MEDLION BIOTECH CO., LTD..
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