Taiwan FDA registration 0495a0fdb3fc04044fc5d4832a662131

"Danyang" Components for in vitro limb prosthetics (unsterilized)

TW: “丹陽” 體外肢體義肢用組件(未滅菌)
Taiwan flagTaiwan·Risk Class 1·DANYANG PROSTHESES FACTORY LIMITED COMPANY·Registered Oct 01, 2021 – Oct 31, 2026Active
Registration details
Analysis ID
0495a0fdb3fc04044fc5d4832a662131
Customs Code
DHA08600441302
Company information
Manufacturer Country
China
Authorized Representative
TEH LIN PROSTHETIC & ORTHOPAEDIC INC.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3420 體外肢體義肢用組件
Import Information
Input;; Chinese goods
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 "Danyang" Components for in vitro limb prosthetics (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0495a0fdb3fc04044fc5d4832a662131 and manufactured by DANYANG PROSTHESES FACTORY LIMITED COMPANY. The authorized representative in Taiwan is TEH LIN PROSTHETIC & ORTHOPAEDIC INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DANYANG PROSTHESES FACTORY LIMITED COMPANY, 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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