Taiwan FDA registration 79e290333b766d655020d9583bc2634f
"Dalian Jintong" manual osteologic surgical instrument (unsterilized)
TW: "大連金通" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·DALIAN KINTON TECHNOLOGY CO., LTD·Registered Feb 12, 2020 – Feb 12, 2025ExpiredRegistration details
- Analysis ID
- 79e290333b766d655020d9583bc2634f
- Customs Code
- DHA09600409201
Company information
- Manufacturer
- DALIAN KINTON TECHNOLOGY CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- PAONAN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 12, 2020
- Expiry Date
- Feb 12, 2025
About this record
Access comprehensive regulatory information for "Dalian Jintong" manual osteologic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 79e290333b766d655020d9583bc2634f and manufactured by DALIAN KINTON TECHNOLOGY CO., LTD. The authorized representative in Taiwan is PAONAN BIOTECH 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