Taiwan FDA registration c4605fc73d670dfc5a94e4d67f991297
"Maxer" Spinal Endoscopic Instruments (Non-Sterile)
TW: "麥克斯" 脊椎內視鏡工具 (未滅菌)
Taiwan·Risk Class 1·MD·MAXER MEDIZINTECHNIK GMBH·Registered Dec 16, 2016 – Dec 16, 2021ExpiredRegistration details
- Analysis ID
- c4605fc73d670dfc5a94e4d67f991297
- License Form
- Ministry of Health Medical Device Import No. 017291
- Customs Code
- DHA09401729102
Company information
- Manufacturer
- MAXER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Ramo International Limited
Product details
- Intended Use
- Limited to the first level identification range of "Arthroscopy (N.1100)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N1100 Arthroscopy
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 16, 2016
- Expiry Date
- Dec 16, 2021
About this record
Access comprehensive regulatory information for "Maxer" Spinal Endoscopic Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c4605fc73d670dfc5a94e4d67f991297 and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is Ramo International Limited.
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