Taiwan FDA registration b687816b413b18264f7c2f926f585f78

"Matilda" in vitro assembly of lower limb prosthesis (unsterilized)

TW: "明德" 體外組裝下肢義肢 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Wande Disabled Equipment Co., Ltd. Zhonghe Factory·Registered Jun 06, 2017 – Jun 06, 2022Cancelled
Registration details
Analysis ID
b687816b413b18264f7c2f926f585f78
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MINGDER MEDICAL ORTHOTICS CO.
Product details
Intended Use
Limited to the first level recognition range of the in vitro assembly of lower limb prosthetics (O.3500) in the management measures for medical devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3500 shades
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Jun 06, 2017
Expiry Date
Jun 06, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Matilda" in vitro assembly of lower limb prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b687816b413b18264f7c2f926f585f78 and manufactured by Wande Disabled Equipment Co., Ltd. Zhonghe Factory. The authorized representative in Taiwan is MINGDER MEDICAL ORTHOTICS CO..

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices