Taiwan FDA registration e68f8297fdda9a8c4d35680f5e091387
“Technomed Europe” Laryngeal Electrode
TW: “泰克諾美特”喉管電極
Taiwan·Risk Class 2·MD·TECHNOMED EUROPE·Registered Apr 04, 2019 – Apr 04, 2024ExpiredRegistration details
- Analysis ID
- e68f8297fdda9a8c4d35680f5e091387
- License Form
- Ministry of Health Medical Device Import No. 032366
- Customs Code
- DHA05603236600
Company information
- Manufacturer
- TECHNOMED EUROPE
- Manufacturer Country
- Netherlands
- Authorized Representative
- SYNGROWTH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1870 Evoked reactive electrical stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 04, 2019
- Expiry Date
- Apr 04, 2024
About this record
Access comprehensive regulatory information for “Technomed Europe” Laryngeal Electrode in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e68f8297fdda9a8c4d35680f5e091387 and manufactured by TECHNOMED EUROPE. The authorized representative in Taiwan is SYNGROWTH CO., LTD..
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