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beka nonpowered sitz bath (Non-Sterile) - Taiwan Registration 4a2c4da437ada82f141be3a91049de63

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 4a2c4da437ada82f141be3a91049de63 and manufactured by BEKA HOSPITEC GMBH. 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 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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4a2c4da437ada82f141be3a91049de63
Registration Details
Taiwan FDA Registration: 4a2c4da437ada82f141be3a91049de63
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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
Cancelled

Registration Details

4a2c4da437ada82f141be3a91049de63

Ministry of Health Medical Device Import No. 020930

DHA09402093004

Company Information

Germany

Product Details

o Equipment for physical medicine

O5125 Non-powered sitz bath

Imported from abroad

Dates and Status

Oct 08, 2019

Oct 08, 2024

Cancellation Information

Logged out

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