"DGH" Keratoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·DGH Technology Inc.·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- 2e9255a3eb34f53bfaacec3b50ddc3f5
- License Form
- Ministry of Health Medical Device Import Registration No. 017752
- Customs Code
- DHA08401775200
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 2e9255a3eb34f53bfaacec3b50ddc3f5 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.