Taiwan FDA registration 6e9f02be32967d28827486abdf180f21
"Maxell" fiber optic light source and vehicle (unsterilized)
TW: "麥克斯爾" 光纖光源及載具(未滅菌)
Taiwan·Risk Class 1·MAXER MEDIZINTECHNIK GMBH·Registered Sep 21, 2012 – Sep 21, 2022CancelledRegistration details
- Analysis ID
- 6e9f02be32967d28827486abdf180f21
- Customs Code
- DHA04401219702
Company information
- Manufacturer
- MAXER MEDIZINTECHNIK GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HIGH TOP MEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.4350 Ear, nose and throat optical fiber light sources and carriers
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2012
- Expiry Date
- Sep 21, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Maxell" fiber optic light source and vehicle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6e9f02be32967d28827486abdf180f21 and manufactured by MAXER MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is HIGH TOP MEDICAL CO., LTD..
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