Taiwan FDA registration ee01a470548447e53ee28248ec00ea81

Phyllis silicone insole (unsterilized)

TW: 菲麗絲矽膠鞋墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Laili Enterprises Co., Ltd·Registered Jul 10, 2009 – Jul 10, 2014Cancelled
Registration details
Analysis ID
ee01a470548447e53ee28248ec00ea81
Customs Code
DHY04300252305
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
TAIWAN STANCH CO., LTD.
Product details
Intended Use
Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3475 Limb fittings
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Jul 10, 2009
Expiry Date
Jul 10, 2014
Cancellation Date
Aug 14, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Phyllis silicone insole (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ee01a470548447e53ee28248ec00ea81 and manufactured by Laili Enterprises Co., Ltd. The authorized representative in Taiwan is TAIWAN STANCH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including R&R MEDICAL CORPORATION LTD., 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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