Taiwan FDA registration bfa7e3a79ac8d27635943185ee101e58

"Trulife" Limb Orthosis (Non-Sterile)

TW: "舒萊芙"肢體裝具(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·TRULIFE INC.·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
bfa7e3a79ac8d27635943185ee101e58
License Form
Ministry of Health Medical Device Import Registration No. 022441
Customs Code
DHA08402244103
Company information
Manufacturer
TRULIFE INC.
Manufacturer Country
United States
Product details
Intended Use
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3475 Body Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2026
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About this record

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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