Pure Global

"Rester" manual stethoscope (unsterilized) - Taiwan Registration 7dd3429ea7c3ff885df1c8f8fedae7d9

Access comprehensive regulatory information for "Rester" manual stethoscope (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7dd3429ea7c3ff885df1c8f8fedae7d9 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is XIN BO ENTERPRISE CO., LTD..

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 Database
Powered by Pure Global AI
89,000+ Devices
7dd3429ea7c3ff885df1c8f8fedae7d9
Registration Details
Taiwan FDA Registration: 7dd3429ea7c3ff885df1c8f8fedae7d9
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Rester" manual stethoscope (unsterilized)
TW: "็‘žๆ–ฏ็‰น"ๆ‰‹ๅ‹•่ฝ่จบๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

7dd3429ea7c3ff885df1c8f8fedae7d9

DHA04401072606

Company Information

Germany

Product Details

Limited to the first-level identification range of the "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.

E Cardiovascular Medicine Science

E.1875 Listening device

import

Dates and Status

Aug 18, 2011

Aug 18, 2016

Jun 26, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ