Taiwan FDA registration 3f4ed02a2276f716796bcdcaad8989e6
"GENTRY WAY" Crutch (Non-Sterile)
TW: "仲群維"醫療用拐杖(未滅菌)
Registration details
- Analysis ID
- 3f4ed02a2276f716796bcdcaad8989e6
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 004530
Company information
- Manufacturer
- GENTRY WAY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENTRY WAY CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Medical Canes (O.3150)".
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3150 Medical cane
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
Access comprehensive regulatory information for "GENTRY WAY" Crutch (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 3f4ed02a2276f716796bcdcaad8989e6 and manufactured by GENTRY WAY CO., LTD.. The authorized representative in Taiwan is GENTRY WAY CO., LTD..
This page provides complete technical specifications, regulatory compliance details. 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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