Taiwan FDA registration 1201fb1cb999a4e1e7c915e23a4601f2
“Orthobion” TSC Posterior/ Transforaminal Lumbar Interbody Fusion Cages
TW: “歐梭比恩”腰椎後側路椎間融合器
Taiwan·Risk Class 2·MD·Orthobion GmbH·Registered Nov 10, 2019 – Nov 10, 2024ExpiredRegistration details
- Analysis ID
- 1201fb1cb999a4e1e7c915e23a4601f2
- License Form
- Ministry of Health Medical Device Import No. 032991
- Customs Code
- DHA05603299107
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)
- N3080 Interbody fusion device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 10, 2019
- Expiry Date
- Nov 10, 2024
About this record
Access comprehensive regulatory information for “Orthobion” TSC Posterior/ Transforaminal Lumbar 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 1201fb1cb999a4e1e7c915e23a4601f2 and manufactured by Orthobion GmbH. The authorized representative in Taiwan is LI MIN BIOTECH CO., LTD..
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