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"Chongwei" Limb orthosis (Non-Sterile)  - Taiwan Registration a0e148023bff0e819d69873b9cfa1ae0

Access comprehensive regulatory information for "Chongwei" 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 a0e148023bff0e819d69873b9cfa1ae0 and manufactured by Heavy Maintenance Rehabilitation Products Co., Ltd. The authorized representative in Taiwan is Heavy Maintenance Rehabilitation Products Co., Ltd.

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a0e148023bff0e819d69873b9cfa1ae0
Registration Details
Taiwan FDA Registration: a0e148023bff0e819d69873b9cfa1ae0
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Device Details

"Chongwei" Limb orthosis (Non-Sterile) 
TW: "重維"肢體裝具 (未滅菌) 
Risk Class 1
MD

Registration Details

a0e148023bff0e819d69873b9cfa1ae0

Ministry of Health Medical Device Manufacturing Registration No. 003394

Company Information

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2026