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"Trulife" Limb Orthosis (Non-Sterile) - Taiwan Registration 21fe12ad170dff3ad67c356253bb7397

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 21fe12ad170dff3ad67c356253bb7397 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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21fe12ad170dff3ad67c356253bb7397
Registration Details
Taiwan FDA Registration: 21fe12ad170dff3ad67c356253bb7397
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Device Details

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

Registration Details

21fe12ad170dff3ad67c356253bb7397

Ministry of Health Medical Device Import No. 022441

DHA09402244102

Company Information

United States

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Apr 01, 2021

Apr 01, 2026

Cancellation Information

Logged out

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