Taiwan FDA registration edd2b433856430d86c35ad613a93b1bb

"HELY AND WEBER" Limb orthosis (Non-Sterile)

TW: "赫莉偉伯" 肢體裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·HELY AND WEBER·Registered Feb 21, 2019 – Feb 21, 2024Cancelled
Registration details
Analysis ID
edd2b433856430d86c35ad613a93b1bb
License Form
Ministry of Health Medical Device Import No. 020112
Customs Code
DHA09402011209
Company information
Manufacturer
HELY AND WEBER
Manufacturer Country
United States
Authorized Representative
ORTHOHEALTH CO., LTD.
Product details
Product Type (Level 1)
o Equipment for physical medicine
Product Type (Level 2)
O3475 Body Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 21, 2019
Expiry Date
Feb 21, 2024
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "HELY AND WEBER" Limb orthosis (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 edd2b433856430d86c35ad613a93b1bb and manufactured by HELY AND WEBER. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELY AND WEBER, 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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