"STRENGTHEN" Nonpowered flotation therapy mattress (Non-Sterile)
Taiwan·Risk Class 1·MD·LINET SPOL. S R. O.·Registered Feb 11, 2020 – Feb 11, 2025Cancelled- Analysis ID
- 8354bc1b6f59c16d82c0cf2fcd000a19
- License Form
- Ministry of Health Medical Device Import No. 021247
- Customs Code
- DHA09402124701
- Manufacturer
- LINET SPOL. S R. O.
- Manufacturer Country
- Czechia
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
- 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
- Feb 11, 2020
- Expiry Date
- Feb 11, 2025
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 8354bc1b6f59c16d82c0cf2fcd000a19 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.