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"Streifeneder" Limb orthosis (Non-Sterile) - Taiwan Registration 7fc08bea0511f1de88680d75c65259c6

Access comprehensive regulatory information for "Streifeneder" 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 7fc08bea0511f1de88680d75c65259c6 and manufactured by STREIFENEDER ORTHO. PRODUCTION GMBH. 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 STREIFENEDER ORTHO. PRODUCTION GMBH, and 3 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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7fc08bea0511f1de88680d75c65259c6
Registration Details
Taiwan FDA Registration: 7fc08bea0511f1de88680d75c65259c6
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Device Details

"Streifeneder" Limb orthosis (Non-Sterile)
TW: "ๅฒ็ฟ ่Šฌ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

7fc08bea0511f1de88680d75c65259c6

Ministry of Health Medical Device Import No. 019969

DHA09401996905

Company Information

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Dec 27, 2018

Dec 27, 2023

Cancellation Information

Logged out

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