beka nonpowered sitz bath (Non-Sterile)
Taiwan·Risk Class 1·MD·BEKA HOSPITEC GMBH·Registered Oct 08, 2019 – Oct 08, 2024Cancelled- Analysis ID
- 4a2c4da437ada82f141be3a91049de63
- License Form
- Ministry of Health Medical Device Import No. 020930
- Customs Code
- DHA09402093004
- Manufacturer
- BEKA HOSPITEC GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Johnson & Johnson Medical Instruments Inc
- 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 08, 2019
- Expiry Date
- Oct 08, 2024
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 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.