Taiwan FDA registration 04dc6ab8c3ec086cb595af2fdea37bbd
"Ermis MedTech" Manual surgical instrument for general use (Non-sterile)
TW: "艾米斯" 一般手術用手動式器械 (未滅菌)
Taiwan·Risk Class 1·MD·Ermis MedTech GmbH·Registered Dec 20, 2018 – Dec 20, 2023ExpiredRegistration details
- Analysis ID
- 04dc6ab8c3ec086cb595af2fdea37bbd
- License Form
- Ministry of Health Medical Device Import No. 019942
- Customs Code
- DHA09401994201
Company information
- Manufacturer
- Ermis MedTech GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- JASPER MEDICAL INSTRUMENTS CO., LTD.
Product details
- 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
Dates and status
- Registration Date
- Dec 20, 2018
- Expiry Date
- Dec 20, 2023
About this record
Access comprehensive regulatory information for "Ermis MedTech" 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 04dc6ab8c3ec086cb595af2fdea37bbd and manufactured by Ermis MedTech GmbH. The authorized representative in Taiwan is JASPER MEDICAL INSTRUMENTS CO., LTD..
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