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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.

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4f708ad69fb02a34a7580ab8c30c7ef2
Registration Details
Taiwan FDA Registration: 4f708ad69fb02a34a7580ab8c30c7ef2
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Device Details

beka nonpowered sitz bath (Non-Sterile)
TW: ๅ€ๅก้žๅ‹•ๅŠ›ๅผๅๆตด(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4f708ad69fb02a34a7580ab8c30c7ef2

Ministry of Health Medical Device Import Registration No. 020930

DHA08402093008

Company Information

Germany

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

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