Taiwan FDA registration 299bdd528d7b9b1363b46c143b728495
“BAAT” Fortilink-TS with TiPlus Technology Transforaminal/Posterior Lumbar Cage
TW: “百適”弗帝希腰椎系統椎間/後方腰椎融合裝置
Taiwan·Risk Class 2·MD·Baat Medical Products B.V.·Registered Jan 19, 2023 – Jan 19, 2028ActiveRegistration details
- Analysis ID
- 299bdd528d7b9b1363b46c143b728495
- License Form
- Ministry of Health Medical Device Import No. 036289
- Customs Code
- DHA05603628902
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
- Jan 19, 2023
- Expiry Date
- Jan 19, 2028
About this record
Access comprehensive regulatory information for “BAAT” Fortilink-TS with TiPlus Technology Transforaminal/Posterior 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 299bdd528d7b9b1363b46c143b728495 and manufactured by Baat Medical Products B.V.. The authorized representative in Taiwan is PARADIGM SPINE TAIWAN LTD..
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