Taiwan FDA registration 79b655683815e602ff859de724cd0a1e
“Medacta” MectaLIF Intervertebral Body Fusion Device
TW: “美達特”美特腰椎椎間融合器
Taiwan·Risk Class 2·MD·Medacta International SA·Registered May 20, 2022 – May 20, 2027ActiveRegistration details
- Analysis ID
- 79b655683815e602ff859de724cd0a1e
- License Form
- Ministry of Health Medical Device Import No. 035479
- Customs Code
- DHA05603547902
Company information
- Manufacturer
- Medacta International SA
- Manufacturer Country
- Switzerland
- Authorized Representative
- LI MIN BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 20, 2022
- Expiry Date
- May 20, 2027
About this record
Access comprehensive regulatory information for “Medacta” MectaLIF Intervertebral Body Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79b655683815e602ff859de724cd0a1e and manufactured by Medacta International SA. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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