Taiwan FDA registration d18c667b946e0297a71b4e79420f7919
“HumanTech” TRISTAN Cervical Interbody Fusion
TW: “優門鐵克”特利斯坦頸椎椎間融合器
Taiwan·Risk Class 2·MD·HumanTech Spine GmbH·Registered Aug 04, 2021 – Aug 04, 2026ActiveRegistration details
- Analysis ID
- d18c667b946e0297a71b4e79420f7919
- License Form
- Ministry of Health Medical Device Import No. 034806
- Customs Code
- DHA05603480609
Company information
- Manufacturer
- HumanTech Spine GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- LI MIN BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 04, 2021
- Expiry Date
- Aug 04, 2026
About this record
Access comprehensive regulatory information for “HumanTech” TRISTAN Cervical Interbody Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d18c667b946e0297a71b4e79420f7919 and manufactured by HumanTech Spine GmbH. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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