Taiwan FDA registration 44bbfd21cbdf91f8b267e58fc20d1845

"FABRICATION" Rehabilitation Devices and Accessories (Non-Sterile)

TW: "斐瑪莉凱訊" 復健用裝具及配件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·FABRICATION ENTERPRISES, INC.·Registered Jun 14, 2017 – Jun 14, 2027Active
Registration details
Analysis ID
44bbfd21cbdf91f8b267e58fc20d1845
License Form
Ministry of Health Medical Device Import No. 017957
Customs Code
DHA09401795701
Company information
Manufacturer Country
United States
Product details
Intended Use
Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Accessories for Prosthetics and Accessories for Accessories for Appliances (O.3025)".
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3025 Accessories for prosthetics and accessories
Import Information
Imported from abroad
Dates and status
Registration Date
Jun 14, 2017
Expiry Date
Jun 14, 2027
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About this record

Access comprehensive regulatory information for "FABRICATION" Rehabilitation Devices and Accessories (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 44bbfd21cbdf91f8b267e58fc20d1845 and manufactured by FABRICATION ENTERPRISES, INC.. The authorized representative in Taiwan is JIH FENG LUNG ENTERPRISES COMPANY LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FABRICATION ENTERPRISES, INC., FABRICATION ENTERPRISES INCORPORATED, and 3 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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