"SPINEART" Orthopedic manual surgical instrument (Non-Sterile)
Taiwan·Risk Class 1·MD·SPINEART·Registered Aug 09, 2017 – Aug 09, 2022Expired- Analysis ID
- 58f4f77ff040da6a8818d8e27f95e9a4
- License Form
- Ministry of Health Medical Device Import No. 018166
- Customs Code
- DHA09401816601
- Manufacturer
- SPINEART
- Manufacturer Country
- Switzerland
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
- 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
- Registration Date
- Aug 09, 2017
- Expiry Date
- Aug 09, 2022
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Access comprehensive regulatory information for "SPINEART" 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 58f4f77ff040da6a8818d8e27f95e9a4 and manufactured by SPINEART. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SPINEART SA, and 2 recent registrations in the same category. 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.