beka nonpowered sitz bath (Non-Sterile) - Taiwan Registration 4f708ad69fb02a34a7580ab8c30c7ef2
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.
Device Details
Registration Details
4f708ad69fb02a34a7580ab8c30c7ef2
Ministry of Health Medical Device Import Registration No. 020930
DHA08402093008
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-powered Sitz Bath (O.5125)".
o Equipment for physical medicine
O5125 Non-powered sitz bath
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2024

