Taiwan FDA registration 85bd4572be38dd81db78ae3d7ca3b3ab

"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 Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
85bd4572be38dd81db78ae3d7ca3b3ab
License Form
Ministry of Health Medical Device Import Registration No. 018121
Customs Code
DHA08401812109
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
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 85bd4572be38dd81db78ae3d7ca3b3ab 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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