Taiwan FDA registration b02fc7a427e98027eac9320485287919
"CarboFix" Orthopedic Manual Surgical Instrument (Non-Sterile)
TW: "卡伯菲" 手動式骨科手術器械 (未滅菌)
Registration details
- Analysis ID
- b02fc7a427e98027eac9320485287919
- License Form
- Ministry of Health Medical Device Import No. 016523
- Customs Code
- DHA09401652302
Company information
- Manufacturer
- CarboFix Orthopedics Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- JOINSMART BIOMEDICAL COMPANY LIMITED
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
- May 12, 2016
- Expiry Date
- May 12, 2026
About this record
Access comprehensive regulatory information for "CarboFix" 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 b02fc7a427e98027eac9320485287919 and manufactured by CarboFix Orthopedics Ltd.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.
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