"APRAMED" Keratoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·APRAMED IND E COM DE APARELHOS MEDICOS LTDA·Registered Oct 11, 2017 – Oct 11, 2022Cancelled- Analysis ID
- f75d6afa3b47d63d4d4d3a069d20d843
- License Form
- Ministry of Health Medical Device Import No. 018390
- Customs Code
- DHA09401839006
- Manufacturer
- APRAMED IND E COM DE APARELHOS MEDICOS LTDA
- Manufacturer Country
- Brazil
- 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 11, 2017
- Expiry Date
- Oct 11, 2022
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for "APRAMED" 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 f75d6afa3b47d63d4d4d3a069d20d843 and manufactured by APRAMED IND E COM DE APARELHOS MEDICOS LTDA. 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 APRAMED IND E COM DE APARELHOS MEDICOS LTDA, 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.