Taiwan FDA registration 19cc272007655f0fcc64a3e5290c5a30
“Orthobion” TSC Anterior Cervical Interbody Fusion Cages
TW: “歐梭比恩”頸椎前路椎間融合器
Taiwan·Risk Class 2·MD·Orthobion GmbH·Registered Aug 22, 2018 – Aug 22, 2028ActiveRegistration details
- Analysis ID
- 19cc272007655f0fcc64a3e5290c5a30
- License Form
- Ministry of Health Medical Device Import No. 031566
- Customs Code
- DHA05603156600
Company information
- Manufacturer
- Orthobion GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- LI MIN BIOTECH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3060 Spine correction fixation between vertebral bodies
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 22, 2018
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for “Orthobion” TSC Anterior Cervical Interbody Fusion Cages in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19cc272007655f0fcc64a3e5290c5a30 and manufactured by Orthobion GmbH. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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