"Exhibition" non-aerated tourniquet (unsterilized)
Taiwan·Risk Class 1·HUI CHIHAN ENTERPRISE CO., LTD.·Registered Mar 09, 2007 – Mar 09, 2012Cancelled- Analysis ID
- 3639d7c4ba70a593661771d14d2bfb07
- Manufacturer
- HUI CHIHAN ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HUI CHIHAN ENTERPRISE CO., LTD.
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.5900 非充氣式止血帶
- Import Information
- Domestic
- Registration Date
- Mar 09, 2007
- Expiry Date
- Mar 09, 2012
- Cancellation Date
- Apr 14, 2014
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Exhibition" non-aerated tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3639d7c4ba70a593661771d14d2bfb07 and manufactured by HUI CHIHAN ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HUI CHIHAN ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HUI CHIHAN ENTERPRISE CO., LTD., and 1 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.