Taiwan FDA registration 944753c8f73d2552f843560f857b0630
“RHYTHMLINK” Disposable Guardian Needle Subdermal Electrodes
TW: “瑞斯林肯”拋棄式皮下針狀電極
Taiwan·Risk Class 2·MD·RHYTHMLINK INTERNATIONAL, LLC·Registered Nov 04, 2022 – Nov 04, 2027ActiveRegistration details
- Analysis ID
- 944753c8f73d2552f843560f857b0630
- License Form
- Ministry of Health Medical Device Import No. 036031
- Customs Code
- DHA05603603102
Company information
- Manufacturer
- RHYTHMLINK INTERNATIONAL, LLC
- Manufacturer Country
- United States
- Authorized Representative
- WELLGROWTH TECHNOLOGY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K1350 Needle Type Electrode
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 04, 2022
- Expiry Date
- Nov 04, 2027
About this record
Access comprehensive regulatory information for “RHYTHMLINK” Disposable Guardian Needle Subdermal Electrodes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 944753c8f73d2552f843560f857b0630 and manufactured by RHYTHMLINK INTERNATIONAL, LLC. The authorized representative in Taiwan is WELLGROWTH TECHNOLOGY CO., LTD..
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