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"TECNOWAY" Limb orthosis (Non-Sterile) - Taiwan Registration 442e5422d7502f2f07c90764a69bcbc9

Access comprehensive regulatory information for "TECNOWAY" 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 442e5422d7502f2f07c90764a69bcbc9 and manufactured by TECNOWAY SRL. 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 TECNOWAY SRL, and 2 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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442e5422d7502f2f07c90764a69bcbc9
Registration Details
Taiwan FDA Registration: 442e5422d7502f2f07c90764a69bcbc9
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Device Details

"TECNOWAY" Limb orthosis (Non-Sterile)
TW: "้ต่ซพๅจ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

442e5422d7502f2f07c90764a69bcbc9

Ministry of Health Medical Device Import No. 019403

DHA09401940307

Company Information

Italy

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Jul 23, 2018

Jul 23, 2023

Cancellation Information

Logged out

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