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"Qinda" belly pad (sterile/unsterilized)  - Taiwan Registration 13d3216eb63071c2abe9dbc7ad8e9736

Access comprehensive regulatory information for "Qinda" belly pad (sterile/unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13d3216eb63071c2abe9dbc7ad8e9736 and manufactured by HOSPITECH MANUFACTURING SERVICES SDN BHD. The authorized representative in Taiwan is TEAM POWER MEDICAL INSTRUMENT LTD..

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13d3216eb63071c2abe9dbc7ad8e9736
Registration Details
Taiwan FDA Registration: 13d3216eb63071c2abe9dbc7ad8e9736
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Device Details

"Qinda" belly pad (sterile/unsterilized) 
TW: "勤達" 腹部墊 (滅菌/未滅菌) 
Risk Class 1
Cancelled

Registration Details

13d3216eb63071c2abe9dbc7ad8e9736

DHA04401189801

Company Information

Product Details

Limited to the first level of identification range of "unabsorbed gauze for in vivo (I.4450)" under the Measures for the Administration of Medical Devices.

I General, Plastic Surgery and Dermatology

I.4450 Non-absorbable filament cloth for internal use

QMS/QSD;; 輸入

Dates and Status

Jun 29, 2012

Jun 29, 2022

Apr 12, 2024

Cancellation Information

Logged out

許可證已逾有效期