"Keiai" Limb orthosis (Non-Sterile) - Taiwan Registration 95034c33cfa6f550033e9cb7071eed35
Access comprehensive regulatory information for "Keiai" 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 95034c33cfa6f550033e9cb7071eed35 and manufactured by KEIAI ORTHOPEDIC APPLIANCE CO., LTD.. The authorized representative in Taiwan is JEN DER P&O APPLIANCES MANUFACTURING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KEIAI ORTHOPEDIC APPLIANCE CO., LTD., and 1 recent registrations in the same category. 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.
Device Details
Registration Details
95034c33cfa6f550033e9cb7071eed35
Ministry of Health Medical Device Import Registration No. 021188
DHA08402118802
Product Details
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
o Equipment for physical medicine
O3475 Body Equipment
Imported from abroad
Dates and Status
Oct 01, 2021
Oct 31, 2025