Taiwan FDA registration 4268076cfc79e0d71d61088e72ad6770

"Streifeneder" External Limb Prosthetic Component (Non-Sterile)

TW: "史黛芬" 體外肢體義肢用組件 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·STREIFENEDER ORTHO. PRODUCTION GMBH·Registered Jun 30, 2017 – Jun 30, 2022Cancelled
Registration details
Analysis ID
4268076cfc79e0d71d61088e72ad6770
License Form
Ministry of Health Medical Device Import No. 018026
Customs Code
DHA09401802601
Company information
Manufacturer Country
Germany
Authorized Representative
KEN DALL ENTERPRISE CO., LTD.
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
Jun 30, 2017
Expiry Date
Jun 30, 2022
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Streifeneder" 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 4268076cfc79e0d71d61088e72ad6770 and manufactured by STREIFENEDER ORTHO. PRODUCTION GMBH. The authorized representative in Taiwan is KEN DALL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including STREIFENEDER ORTHO. PRODUCTION GMBH, and 2 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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