Taiwan FDA registration 1f4e4d9d0e7ca6116908bd4e6df3d946
“Maquet” VOLISTA Surgical Light
TW: “邁柯唯”手術燈
Taiwan·Risk Class 2·MD·MAQUET SAS·Registered Sep 13, 2013 – Sep 13, 2028ActiveRegistration details
- Analysis ID
- 1f4e4d9d0e7ca6116908bd4e6df3d946
- License Form
- Ministry of Health Medical Device Import No. 025415
- Customs Code
- DHA05602541506
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 and plastic surgical devices
- Product Type (Level 2)
- I4580 Surgical light
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 13, 2013
- Expiry Date
- Sep 13, 2028
About this record
Access comprehensive regulatory information for “Maquet” VOLISTA 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 1f4e4d9d0e7ca6116908bd4e6df3d946 and manufactured by MAQUET SAS. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices