"Taica" Nonpowered flotation therapy mattress (Non-Sterile)
Taiwan·Risk Class 1·MD·TAICA CORPORATION·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- cbb8c817d19c409e77b19b99ec7e0d2f
- License Form
- Ministry of Health Medical Device Import Registration No. 017395
- Customs Code
- DHA08401739502
- Manufacturer
- TAICA CORPORATION
- Manufacturer Country
- Japan
- Authorized Representative
- FUROTO MEDICAL & WELFARE 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 "Taica" 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 cbb8c817d19c409e77b19b99ec7e0d2f and manufactured by TAICA CORPORATION. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TAICA CORPORATION, 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.