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“Hallufix”Splint for Hallux Valgus(Non-Sterile) - Taiwan Registration 59f6584b6665ff0b48cb5c8557283729

Access comprehensive regulatory information for “Hallufix”Splint for Hallux Valgus(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 59f6584b6665ff0b48cb5c8557283729 and manufactured by HALLUFIX AG. The authorized representative in Taiwan is LINKSEAS TRADING CO., 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.

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59f6584b6665ff0b48cb5c8557283729
Registration Details
Taiwan FDA Registration: 59f6584b6665ff0b48cb5c8557283729
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Device Details

“Hallufix”Splint for Hallux Valgus(Non-Sterile)
TW: “好樂適”拇趾外翻矯正器 (未滅菌)
Risk Class 1
MD

Registration Details

59f6584b6665ff0b48cb5c8557283729

Ministry of Health Medical Device Import Registration No. 007424

DHA08400742403

Company Information

Germany

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, 2024