"Li Tong" Non-AC Electric Patient Lift (Unsterilized)
Taiwan·Risk Class 1·RIFTON EQUIPMENT·Registered Oct 22, 2012 – Oct 22, 2022Cancelled- Analysis ID
- b7fc40522874d0e51fbb5a248e950ff6
- Customs Code
- DHA04401228805
- Manufacturer
- RIFTON EQUIPMENT
- Manufacturer Country
- United States
- Authorized Representative
- BIOSYSTEMS INC.
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Non-AC Electric Patient Lift (J.5510)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5510 Non-AC electric patient lifts
- Import Information
- import
- Registration Date
- Oct 22, 2012
- Expiry Date
- Oct 22, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Li Tong" Non-AC Electric Patient Lift (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b7fc40522874d0e51fbb5a248e950ff6 and manufactured by RIFTON EQUIPMENT. The authorized representative in Taiwan is BIOSYSTEMS INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RIFTON EQUIPMENT, 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.