Taiwan FDA registration 4b8b1ac1cf7b21b79bf22a84933a4c5d
“Lutronic”CoreLevee Electromagnetic Stimulator System
TW: “璐霓可”磁波刺激系統
Taiwan·Risk Class 2·MD·LUTRONIC CORPORATION·Registered Oct 08, 2022 – Oct 08, 2027ActiveRegistration details
- Analysis ID
- 4b8b1ac1cf7b21b79bf22a84933a4c5d
- License Form
- Ministry of Health Medical Device Import No. 035962
- Customs Code
- DHA05603596202
Company information
- Manufacturer
- LUTRONIC CORPORATION
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- K&C MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 08, 2022
- Expiry Date
- Oct 08, 2027
About this record
Access comprehensive regulatory information for “Lutronic”CoreLevee Electromagnetic Stimulator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b8b1ac1cf7b21b79bf22a84933a4c5d and manufactured by LUTRONIC CORPORATION. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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