Taiwan FDA registration 18d1b0b0181cf652bbe42da821649360
Components for in vitro prosthetics of "Eslone" (unsterilized)
TW: “艾斯隆”體外肢體義肢用組件(未滅菌)
Taiwan·Risk Class 1·RSL STEEPER·Registered Mar 28, 2011 – Mar 28, 2021CancelledRegistration details
- Analysis ID
- 18d1b0b0181cf652bbe42da821649360
- Customs Code
- DHA04401009306
Company information
- Manufacturer
- RSL STEEPER
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CHENG CHUAN P&O CO., LTD.
Product details
- 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
- import
Dates and status
- Registration Date
- Mar 28, 2011
- Expiry Date
- Mar 28, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Components for in vitro prosthetics of "Eslone" (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 18d1b0b0181cf652bbe42da821649360 and manufactured by RSL STEEPER. The authorized representative in Taiwan is CHENG CHUAN P&O CO., LTD..
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