Taiwan FDA registration a922317c0b696a1554fb41c33efe095d
“KOIBIG” Transcutaneous Electrical Modulation System
TW: “科比”經皮神經電刺激器
Taiwan·Risk Class 2·MD·Mediver Inc.·Registered Oct 21, 2021 – Oct 21, 2026ActiveRegistration details
- Analysis ID
- a922317c0b696a1554fb41c33efe095d
- License Form
- Ministry of Health Medical Device Import No. 034978
- Customs Code
- DHA05603497802
Company information
- Manufacturer
- Mediver Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SERVICETECH INTERNATIONAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 21, 2021
- Expiry Date
- Oct 21, 2026
About this record
Access comprehensive regulatory information for “KOIBIG” Transcutaneous Electrical Modulation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a922317c0b696a1554fb41c33efe095d and manufactured by Mediver Inc.. The authorized representative in Taiwan is SERVICETECH INTERNATIONAL INC..
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