"JOSEF HEISS" Manual surgical instrument for general use (Non-Sterile)
Taiwan·Risk Class 1·MD·JOSEF HEISS MEDICAL GMBH·Registered May 23, 2016 – May 23, 2021Expired- Analysis ID
- 8c7e2be9f433d20c9297a75c23b9a63e
- License Form
- Ministry of Health Medical Device Import No. 016568
- Customs Code
- DHA09401656801
- Manufacturer
- JOSEF HEISS MEDICAL GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- Liren Equipment Factory Co., Ltd
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
- Registration Date
- May 23, 2016
- Expiry Date
- May 23, 2021
Top companies providing products similar to ""JOSEF HEISS" Manual surgical instrument for general use (Non-Sterile)"
Recently registered similar products
Access comprehensive regulatory information for "JOSEF HEISS" Manual surgical instrument for general use (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 8c7e2be9f433d20c9297a75c23b9a63e and manufactured by JOSEF HEISS MEDICAL GMBH. The authorized representative in Taiwan is Liren Equipment Factory Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JOSEF HEISS MEDICAL GMBH, 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.