Taiwan FDA registration 1bb932810fcf489249b1c71976918f0d

"Jen-Der" Crutch (Non-Sterile)

TW: "正德" 醫療用柺杖 (未滅菌)

Taiwan·Risk Class 1·MD·JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: 1bb932810fcf489249b1c71976918f0d
License Form: Ministry of Health Medical Device Manufacturing Registration No. 006261

Company information

Manufacturer: JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Canes (O.3150)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3150 Medical cane
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for "Jen-Der" Crutch (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 1bb932810fcf489249b1c71976918f0d and manufactured by JEN DER P&O APPLIANCES MANUFACTURING CO., LTD.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..

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