Taiwan FDA registration 289bfeb9cbe62b648a2d6543e7bdfef5
"HMD Omni Pro" Manual Stethoscope (Non-sterile)
TW: "杏昌" 手動聽診器 (未滅菌)
Taiwan·Risk Class 1·MD·HMD HK LTD·Registered Mar 12, 2020 – Mar 12, 2025ExpiredRegistration details
- Analysis ID
- 289bfeb9cbe62b648a2d6543e7bdfef5
- License Form
- Ministry of Health Medical Device Import No. 021362
- Customs Code
- DHA09402136201
Company information
- Manufacturer
- HMD HK LTD
- Manufacturer Country
- Hong Kong
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- Limited to the first-level identification range of the "stethoscope (E.1875)" of the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1875 stethoscope
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 12, 2020
- Expiry Date
- Mar 12, 2025
About this record
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.
Free DatabasePowered by Pure Global AI89,000+ Devices