"ArjoHuntleigh" Nonpowered flotation therapy mattress (non-sterile)
Taiwan·Risk Class 1·MD·ARJOHUNTLEIGH POLSKA SP. ZO. O.·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- 736145b9cf5c7978e8df68b6d0ff25f4
- License Form
- Ministry of Health Medical Device Import Registration No. 017618
- Customs Code
- DHA08401761809
- Manufacturer
- ARJOHUNTLEIGH POLSKA SP. ZO. O.
- Manufacturer Country
- Poland
- Authorized Representative
- GETINGE GROUP TAIWAN CO., LTD.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5150 Non-powered treatment mattress
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "ArjoHuntleigh" Nonpowered flotation therapy mattress (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 736145b9cf5c7978e8df68b6d0ff25f4 and manufactured by ARJOHUNTLEIGH POLSKA SP. ZO. O.. The authorized representative in Taiwan is GETINGE GROUP TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARJOHUNTLEIGH POLSKA SP. ZO. O., and 2 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.