Taiwan FDA registration c5fe02b0b97f5318f16c47fc2d600abe
"Mai Kewei" illuminated secondary tube surgical light
TW: “邁柯唯”發光二級管手術燈
Taiwan·Risk Class 2·MAQUET SAS·Registered Aug 06, 2009 – Aug 06, 2029ActiveRegistration details
- Analysis ID
- c5fe02b0b97f5318f16c47fc2d600abe
- Customs Code
- DHA00602009700
Company information
- Manufacturer
- MAQUET SAS
- Manufacturer Country
- France
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4580 Surgical lamp
- Import Information
- import
Dates and status
- Registration Date
- Aug 06, 2009
- Expiry Date
- Aug 06, 2029
About this record
Access comprehensive regulatory information for "Mai Kewei" illuminated secondary tube surgical light in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c5fe02b0b97f5318f16c47fc2d600abe and manufactured by MAQUET SAS. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
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