Taiwan FDA registration 35d16ff8d09e9bf48580f47a0f023ba2
“BAAT” Fortilink-L with TiPlus Technology Lateral Lumbar Cage
TW: “百適”弗帝希腰椎系統側位融合裝置
Taiwan·Risk Class 2·MD·Baat Medical Products B.V.·Registered Dec 21, 2022 – Dec 21, 2027ActiveRegistration details
- Analysis ID
- 35d16ff8d09e9bf48580f47a0f023ba2
- License Form
- Ministry of Health Medical Device Import No. 036141
- Customs Code
- DHA05603614106
Company information
- Manufacturer
- Baat Medical Products B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- PARADIGM SPINE TAIWAN 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
- Dec 21, 2022
- Expiry Date
- Dec 21, 2027
About this record
Access comprehensive regulatory information for “BAAT” Fortilink-L with TiPlus Technology Lateral Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 35d16ff8d09e9bf48580f47a0f023ba2 and manufactured by Baat Medical Products B.V.. The authorized representative in Taiwan is PARADIGM SPINE TAIWAN LTD..
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