Taiwan FDA registration 404f3b44ae9106e93fa45c6e404e6cc0

"Trulife" External Limb Prosthetic Component (Non-Sterile)

TW: "真活" 體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TRULIFE·Registered Jul 27, 2017 – Jul 27, 2022Cancelled
Registration details
Analysis ID
404f3b44ae9106e93fa45c6e404e6cc0
License Form
Ministry of Health Medical Device Import No. 018121
Customs Code
DHA09401812105
Company information
Manufacturer
TRULIFE
Manufacturer Country
United States
Authorized Representative
UHEALTH COMPANY LIMITED
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3420 Components for in vitro limb prosthetics
Import Information
Imported from abroad
Dates and status
Registration Date
Jul 27, 2017
Expiry Date
Jul 27, 2022
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Trulife" External Limb Prosthetic Component (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 404f3b44ae9106e93fa45c6e404e6cc0 and manufactured by TRULIFE. The authorized representative in Taiwan is UHEALTH COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRULIFE, 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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