Taiwan FDA registration a6226baded0ea00dd0903a92da5dbc88

"WELL-DAY" Limb orthosis (Non-Sterile)

TW: "晶晏" 肢體裝具 (未滅菌)

Taiwan·Risk Class 1·MD·WELL-DAY INTERNATIONAL LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: a6226baded0ea00dd0903a92da5dbc88
License Form: Ministry of Health Medical Device Manufacturing Registration No. 006286

Company information

Manufacturer: WELL-DAY INTERNATIONAL LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: WELL-DAY INTERNATIONAL 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 Equipment for physical medicine
Product Type (Level 2): O3475 Body Equipment
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 "WELL-DAY" Limb orthosis (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 a6226baded0ea00dd0903a92da5dbc88 and manufactured by WELL-DAY INTERNATIONAL LTD.. The authorized representative in Taiwan is WELL-DAY INTERNATIONAL 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.