Taiwan FDA registration d1c258262854df084075ddbf49045273
“maxmore” spine Endoscopes
TW: “麥克斯摩爾”脊椎內視鏡
Taiwan·Risk Class 2·MD·HOOGLAND SPINE PRODUCTS GMBH·Registered May 16, 2020 – May 16, 2025ExpiredRegistration details
- Analysis ID
- d1c258262854df084075ddbf49045273
- License Form
- Ministry of Health Medical Device Import No. 033642
- Customs Code
- DHA05603364200
Company information
- Manufacturer
- HOOGLAND SPINE PRODUCTS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- CHIN I PAO 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)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 16, 2020
- Expiry Date
- May 16, 2025
About this record
Access comprehensive regulatory information for “maxmore” spine Endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d1c258262854df084075ddbf49045273 and manufactured by HOOGLAND SPINE PRODUCTS GMBH. The authorized representative in Taiwan is CHIN I PAO CO., LTD..
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