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"ALLARD" Limb Orthosis (Non-Sterile) - Taiwan Registration 026323958a3a121dd7b60a9e41cdca63

Access comprehensive regulatory information for "ALLARD" 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 026323958a3a121dd7b60a9e41cdca63 and manufactured by ALLARD USA INC.. The authorized representative in Taiwan is CHENG CHUAN P&O 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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026323958a3a121dd7b60a9e41cdca63
Registration Details
Taiwan FDA Registration: 026323958a3a121dd7b60a9e41cdca63
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Device Details

"ALLARD" Limb Orthosis (Non-Sterile)
TW: "่‰พๆ‹‰ๅพท" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

026323958a3a121dd7b60a9e41cdca63

Ministry of Health Medical Device Import No. 013746

DHA09401374607

Company Information

United States

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Jan 03, 2014

Jan 03, 2024

Cancellation Information

Logged out

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