Taiwan FDA registration 27b08bde46cb715fc20fce8cecb91c29
"Lemmy" magnetic wave stimulator
TW: “樂密”磁波刺激器
Registration details
- Analysis ID
- 27b08bde46cb715fc20fce8cecb91c29
- Customs Code
- DHA05603481701
Company information
- Manufacturer
- Remed Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Xintai Biotech Co., Ltd
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience;;O Physical Medical Sciences
- Product Type (Level 2)
- K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
- Import Information
- import
Dates and status
- Registration Date
- Aug 13, 2021
- Expiry Date
- Aug 13, 2026
About this record
Access comprehensive regulatory information for "Lemmy" magnetic wave stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27b08bde46cb715fc20fce8cecb91c29 and manufactured by Remed Co., Ltd.. The authorized representative in Taiwan is Xintai Biotech Co., Ltd.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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