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"Riester" Manual Stethoscope (Non-Sterile) - Taiwan Registration ef9077aeed2fc0673f81ab2dff7b353f

Access comprehensive regulatory information for "Riester" Manual Stethoscope (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 ef9077aeed2fc0673f81ab2dff7b353f and manufactured by Rudolf Riester GmbH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY 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.

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ef9077aeed2fc0673f81ab2dff7b353f
Registration Details
Taiwan FDA Registration: ef9077aeed2fc0673f81ab2dff7b353f
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Device Details

"Riester" Manual Stethoscope (Non-Sterile)
TW: "็‘žๅธ" ๆ‰‹ๅ‹•่ฝ่จบๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ef9077aeed2fc0673f81ab2dff7b353f

Ministry of Health Medical Device Import No. 016761

DHA09401676105

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 devices

E1875 stethoscope

Imported from abroad

Dates and Status

Jul 11, 2016

Jul 11, 2026