"DGH" Keratoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·DGH Technology Inc.·Registered Apr 24, 2017 – Apr 24, 2022Cancelled- Analysis ID
- 91c4a39e81030c3999a2eefb445bdff7
- License Form
- Ministry of Health Medical Device Import No. 017752
- Customs Code
- DHA09401775209
- Manufacturer
- DGH Technology Inc.
- Manufacturer Country
- United States
- 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 24, 2017
- Expiry Date
- Apr 24, 2022
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "DGH" 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 91c4a39e81030c3999a2eefb445bdff7 and manufactured by DGH Technology Inc.. 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 DGH Technology Inc., 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.