“ARJO” Patient Lifting (Non-Sterile)
Taiwan·Risk Class 1·MD·ARJOHUNTLEIGH POLSKA SP. ZO. O.·Registered Aug 28, 2017 – Aug 28, 2022Expired- Analysis ID
- 055cf84ca32967d09bbd203382330fd1
- License Form
- Ministry of Health Medical Device Import No. 018241
- Customs Code
- DHA09401824102
- Manufacturer
- ARJOHUNTLEIGH POLSKA SP. ZO. O.
- Manufacturer Country
- Poland
- Authorized Representative
- YI RUEI ENTERPRISE CO., LTD.
- 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)
- J5510 Non-AC Electric Patient Lift
- Import Information
- Imported from abroad
- Registration Date
- Aug 28, 2017
- Expiry Date
- Aug 28, 2022
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Access comprehensive regulatory information for “ARJO” Patient Lifting (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 055cf84ca32967d09bbd203382330fd1 and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is YI RUEI ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJO INTERNATIONAL AB, 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.