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"Keiai" Limb orthosis (Non-Sterile) - Taiwan Registration 68333731d4449046886c26e800134795

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 68333731d4449046886c26e800134795 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.

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68333731d4449046886c26e800134795
Registration Details
Taiwan FDA Registration: 68333731d4449046886c26e800134795
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Device Details

"Keiai" Limb orthosis (Non-Sterile)
TW: "ๅ•Ÿๆ„›" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

68333731d4449046886c26e800134795

Ministry of Health Medical Device Import No. 021188

DHA09402118808

Company Information

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Jan 15, 2020

Jan 15, 2025

Cancellation Information

Logged out

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