Taiwan FDA registration f83f773781f3add5b4f6e563b42920bf

"OG" Mechanical wheelchair (non-sterile)

TW: "歐居" 機械式輪椅 (未滅菌)

Taiwan·Risk Class 1·MD·OG Wellness Technologies CO., LTD., OKU FACTORY·Registered May 09, 2018 – May 09, 2023Expired

Registration details

Analysis ID: f83f773781f3add5b4f6e563b42920bf
License Form: Ministry of Health Medical Device Import No. 019034
Customs Code: DHA09401903402

Company information

Manufacturer: OG Wellness Technologies CO., LTD., OKU FACTORY
Manufacturer Country: Japan
Authorized Representative: AMPLE MEDICAL INSTRUMENTS CO., LTD.

Product details

Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3850 mechanical wheelchair
Import Information: Imported from abroad

Dates and status

Registration Date: May 09, 2018
Expiry Date: May 09, 2023
Cancellation Date: Mar 27, 2023

About this record

Access comprehensive regulatory information for "OG" Mechanical 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 f83f773781f3add5b4f6e563b42920bf and manufactured by OG Wellness Technologies CO., LTD., OKU FACTORY. The authorized representative in Taiwan is AMPLE MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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.