"Regemini" manual patient transport device (unsterilized)
Taiwan·Risk Class 1·CHANGZHOU LAIJIE HEALTH MATERIALS CO., LTD.·Registered Mar 21, 2019 – Mar 21, 2024Cancelled- Analysis ID
- e794899bdb47d8c2f262e009483e81b3
- Customs Code
- DHA09600373308
- Manufacturer
- CHANGZHOU LAIJIE HEALTH MATERIALS CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- FUROTO MEDICAL & WELFARE CO., LTD.
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6785 Manual Patient Conveying Device
- Import Information
- Input;; Chinese goods
- Registration Date
- Mar 21, 2019
- Expiry Date
- Mar 21, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Regemini" manual patient transport device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e794899bdb47d8c2f262e009483e81b3 and manufactured by CHANGZHOU LAIJIE HEALTH MATERIALS CO., LTD.. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CHANGZHOU LAIJIE HEALTH MATERIALS CO., LTD., and 1 recent registrations in the same category. 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.