Taiwan FDA registration bd47c48c79a69365f50b3c7fa7fd6b31
“Laborie” Biofeedback and Stimulation System
TW: “雷柏瑞”生物回饋及電刺激系統
Taiwan·Risk Class 2·MD·LABORIE MEDICAL TECHNOLOGIES CANADA ULC.·Registered Oct 22, 2013 – Oct 22, 2023ExpiredRegistration details
- Analysis ID
- bd47c48c79a69365f50b3c7fa7fd6b31
- License Form
- Ministry of Health Medical Device Import No. 025505
- Customs Code
- DHA05602550507
Company information
- Manufacturer
- LABORIE MEDICAL TECHNOLOGIES CANADA ULC.
- Manufacturer Country
- Canada
- Authorized Representative
- MEDEN INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5320 Non-implantable electronic urination homemade device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 22, 2013
- Expiry Date
- Oct 22, 2023
About this record
Access comprehensive regulatory information for “Laborie” Biofeedback and Stimulation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd47c48c79a69365f50b3c7fa7fd6b31 and manufactured by LABORIE MEDICAL TECHNOLOGIES CANADA ULC.. The authorized representative in Taiwan is MEDEN INTERNATIONAL INC..
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