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"Trulife" Limb Orthosis (Non-Sterile) - Taiwan Registration bfa7e3a79ac8d27635943185ee101e58

Access comprehensive regulatory information for "Trulife" 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 bfa7e3a79ac8d27635943185ee101e58 and manufactured by TRULIFE INC.. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRULIFE INC., 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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bfa7e3a79ac8d27635943185ee101e58
Registration Details
Taiwan FDA Registration: bfa7e3a79ac8d27635943185ee101e58
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Device Details

"Trulife" Limb Orthosis (Non-Sterile)
TW: "่ˆ’่Š่Š™"่‚ข้ซ”่ฃๅ…ท(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bfa7e3a79ac8d27635943185ee101e58

Ministry of Health Medical Device Import Registration No. 022441

DHA08402244103

Company Information

United States

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, 2026

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