Taiwan FDA registration e90fc6232afb757f3e490ff9f057be28
LP limb equipment (unsterilized)
TW: LP肢體裝具 (未滅菌)
Taiwan·Risk Class 1·PLUS MEDITECH CO., LTD.·Registered Dec 10, 2013 – Dec 10, 2023CancelledRegistration details
- Analysis ID
- e90fc6232afb757f3e490ff9f057be28
Company information
- Manufacturer
- PLUS MEDITECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PLUS MEDITECH CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 10, 2013
- Expiry Date
- Dec 10, 2023
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for LP limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e90fc6232afb757f3e490ff9f057be28 and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH CO., LTD..
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