beka nonpowered sitz bath (Non-Sterile)
Taiwan·Risk Class 1·MD·BEKA HOSPITEC GMBH·Registered Oct 01, 2021 – Oct 31, 2024Expired- Analysis ID
- 4f708ad69fb02a34a7580ab8c30c7ef2
- License Form
- Ministry of Health Medical Device Import Registration No. 020930
- Customs Code
- DHA08402093008
- Manufacturer
- BEKA HOSPITEC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Johnson & Johnson Medical Devices, Inc
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Sitz Bath (O.5125)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5125 Non-powered sitz bath
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2024
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Access comprehensive regulatory information for beka nonpowered sitz bath (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 4f708ad69fb02a34a7580ab8c30c7ef2 and manufactured by BEKA HOSPITEC GMBH. The authorized representative in Taiwan is Johnson & Johnson Medical Devices, Inc.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BEKA HOSPITEC GMBH, 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.