"Port" components for in vitro limb prosthetics (unsterilized)
Taiwan·Risk Class 1·SHANGHAI BESTIRRED REHABILITATION EQUIPMENT CO., LTD.·Registered Nov 14, 2017 – Nov 14, 2022Cancelled- Analysis ID
- 4b95ab97f6828dc202174d14847774df
- Customs Code
- DHA09600327007
- Manufacturer Country
- China
- Authorized Representative
- KEN DALL ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level recognition range of components for in vitro limb prosthetics (O.3420) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3420 體外肢體義肢用組件
- Import Information
- Input;; Chinese goods
- Registration Date
- Nov 14, 2017
- Expiry Date
- Nov 14, 2022
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "Port" components for in vitro limb prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4b95ab97f6828dc202174d14847774df and manufactured by SHANGHAI BESTIRRED REHABILITATION EQUIPMENT CO., LTD.. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHANGHAI BESTIRRED REHABILITATION EQUIPMENT CO., LTD., 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.