Taiwan FDA registration c6f568ea805655eaf2ed45ce302c135b
“Hausmann” Plinth (Non-Sterile)
TW: “哈士門” 治療檯 (未滅菌)
Taiwan·Risk Class 1·MD·HAUSMANN INDUSTREIS, INC.·Registered Nov 11, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- c6f568ea805655eaf2ed45ce302c135b
- License Form
- Ministry of Health Medical Device Import Registration No. a00022
- Customs Code
- DHA084a0002207
Company information
- Manufacturer
- HAUSMANN INDUSTREIS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O3520 treatment unit
Dates and status
- Registration Date
- Nov 11, 2021
- Expiry Date
- Oct 31, 2023
- Cancellation Date
- Dec 07, 2022
About this record
Access comprehensive regulatory information for “Hausmann” Plinth (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 c6f568ea805655eaf2ed45ce302c135b and manufactured by HAUSMANN INDUSTREIS, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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