"STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile)
Taiwan·Risk Class 1·MD·LINET SPOL. S R. O.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- ad2a57989617e6302f8a03c9ace1dbaf
- License Form
- Ministry of Health Medical Device Import Registration No. 021247
- Customs Code
- DHA08402124702
- Manufacturer
- LINET SPOL. S R. O.
- Manufacturer Country
- Czechia
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Therapeutic Mattresses (J.5150)".
- 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, 2025
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Access comprehensive regulatory information for "STRENGTHEN" 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 ad2a57989617e6302f8a03c9ace1dbaf and manufactured by LINET SPOL. S R. O.. The authorized representative in Taiwan is Johnson & Johnson Medical Instruments Inc.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including LINET SPOL. S R. O., 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.