Taiwan FDA registration 38747deea40e83da565da70549b04f33

"RSL STEEPER" External limb prosthetic component (Non-Sterile)

TW: "愛斯隆史替波" 體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RSL STEEPER·Registered Oct 01, 2021 – Oct 31, 2022Cancelled
Registration details
Analysis ID
38747deea40e83da565da70549b04f33
License Form
Ministry of Health Medical Device Import Registration No. 017255
Customs Code
DHA08401725502
Company information
Manufacturer
RSL STEEPER
Manufacturer Country
United Kingdom
Authorized Representative
TEH LIN PROSTHETIC & ORTHOPAEDIC INC.
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3420 Components for in vitro limb prosthetics
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "RSL STEEPER" External limb prosthetic component (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 38747deea40e83da565da70549b04f33 and manufactured by RSL STEEPER. 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 RSL STEEPER, 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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