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3M LITTMANN 聽診器 (未滅菌) - Taiwan Registration 0074c50afb506a42fbee85d6cf4d5b3b

Access comprehensive regulatory information for 3M LITTMANN 聽診器 (未滅菌) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0074c50afb506a42fbee85d6cf4d5b3b and manufactured by 3M COMPANY, 3M CAMBRIDGE PLANT. The authorized representative in Taiwan is Taiwan Minnesota Mining Manufacturing Co., Ltd.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including 3M COMPANY, 3M HEALTH CARE, and 2 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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0074c50afb506a42fbee85d6cf4d5b3b
Registration Details
Taiwan FDA Registration: 0074c50afb506a42fbee85d6cf4d5b3b
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Device Details

3M LITTMANN 聽診器 (未滅菌)
Risk Class 1
Cancelled

Registration Details

0074c50afb506a42fbee85d6cf4d5b3b

DHA04400010701

Company Information

Product Details

A manual stethoscope is a device used to express sounds related to the heart, arteries, veins and internal organs.

E Cardiovascular Medicine Science

E.1875 Listening device

import

Dates and Status

May 26, 2005

May 26, 2015

Apr 25, 2018

Cancellation Information

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