Taiwan FDA registration 68e225d5773e2608befc7fb3d9776ffc

“Wonderful” Manual Wheelchair (Non-Sterile)

TW: “穩得福”手動輪椅(未滅菌)

Taiwan·Risk Class 1·MD·SHANGHAI SHUNLONG PTE CO., LTD.·Registered Dec 26, 2018 – Dec 26, 2023Expired

Registration details

Analysis ID: 68e225d5773e2608befc7fb3d9776ffc
License Form: Ministry of Health Medical Device Land Transport No. 003648
Customs Code: DHA09600364804

Company information

Manufacturer: SHANGHAI SHUNLONG PTE CO., LTD.
Manufacturer Country: China
Authorized Representative: FUGI ASSISTIVE DEVICE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Mechanical Wheelchair (O.3850)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3850 mechanical wheelchair
Import Information: Imported from abroad; Made in China

Dates and status

Registration Date: Dec 26, 2018
Expiry Date: Dec 26, 2023

About this record

Access comprehensive regulatory information for “Wonderful” Manual Wheelchair (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 68e225d5773e2608befc7fb3d9776ffc and manufactured by SHANGHAI SHUNLONG PTE CO., LTD.. The authorized representative in Taiwan is FUGI ASSISTIVE DEVICE CO., LTD..

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