"NEITZ" Keratoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·NEITZ INSTRUMENTS CO., LTD.·Registered Apr 16, 2019 – Apr 16, 2024Cancelled- Analysis ID
- f5f239a6819b72e1cc0bfec0c80ab707
- License Form
- Ministry of Health Medical Device Import No. 020318
- Customs Code
- DHA09402031803
- Manufacturer
- NEITZ INSTRUMENTS CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Kangcheng Biomedical Technology Co., Ltd
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1350 Keatoscope
- Import Information
- Imported from abroad
- Registration Date
- Apr 16, 2019
- Expiry Date
- Apr 16, 2024
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "NEITZ" Keratoscope (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 f5f239a6819b72e1cc0bfec0c80ab707 and manufactured by NEITZ INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Kangcheng Biomedical Technology Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NEITZ INSTRUMENTS 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.