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"HMD Omni Pro" Manual Stethoscope (Non-sterile) - Taiwan Registration 289bfeb9cbe62b648a2d6543e7bdfef5

Access comprehensive regulatory information for "HMD Omni Pro" 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 289bfeb9cbe62b648a2d6543e7bdfef5 and manufactured by HMD HK LTD. The authorized representative in Taiwan is HI-CLEARANCE INC..

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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289bfeb9cbe62b648a2d6543e7bdfef5
Registration Details
Taiwan FDA Registration: 289bfeb9cbe62b648a2d6543e7bdfef5
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Device Details

"HMD Omni Pro" Manual Stethoscope (Non-sterile)
TW: "ๆๆ˜Œ" ๆ‰‹ๅ‹•่ฝ่จบๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

289bfeb9cbe62b648a2d6543e7bdfef5

Ministry of Health Medical Device Import No. 021362

DHA09402136201

Company Information

Hong Kong

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

Mar 12, 2020

Mar 12, 2025