"Trulife" Limb Orthosis (Non-Sterile)
- Analysis ID
- bfa7e3a79ac8d27635943185ee101e58
- License Form
- Ministry of Health Medical Device Import Registration No. 022441
- Customs Code
- DHA08402244103
- Manufacturer
- TRULIFE INC.
- Manufacturer Country
- United States
- Authorized Representative
- Heavy Maintenance Rehabilitation Products Co., Ltd
- 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
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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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.