Taiwan FDA registration 5fc4061b67c361f4b20e9d96a23d61ac
“Invivo” Magnetic Resonance Imaging Coils
TW: “英維沃” 磁振造影線圈
Taiwan·Risk Class 2·MD·INVIVO CORPORATION·Registered Apr 19, 2021 – Apr 19, 2026ExpiredRegistration details
- Analysis ID
- 5fc4061b67c361f4b20e9d96a23d61ac
- License Form
- Ministry of Health Medical Device Import No. 034504
- Customs Code
- DHA05603450406
Company information
- Manufacturer
- INVIVO CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1000 Magnetic Resonance Diagnostic Unit
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 19, 2021
- Expiry Date
- Apr 19, 2026
About this record
Access comprehensive regulatory information for “Invivo” Magnetic Resonance Imaging Coils in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5fc4061b67c361f4b20e9d96a23d61ac and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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