"APRAMED" Keratoscope (Non-Sterile)
Taiwan·Risk Class 1·MD·APRAMED IND E COM DE APARELHOS MEDICOS LTDA·Registered Oct 01, 2021 – Oct 31, 2023Expired- Analysis ID
- de21213d988e7caf6f2389feade2be89
- License Form
- Ministry of Health Medical Device Import Registration No. 018390
- Customs Code
- DHA08401839000
- Manufacturer
- APRAMED IND E COM DE APARELHOS MEDICOS LTDA
- Manufacturer Country
- Brazil
- Authorized Representative
- Kangcheng Biomedical Technology Co., Ltd
- Intended Use
- Limited to the first level identification range of the "Corneatoscope (M.1350)" of the Measures for the Administration of Medical Devices.
- 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, 2023
Top companies providing products similar to ""APRAMED" Keratoscope (Non-Sterile)"
Recently registered similar products
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 de21213d988e7caf6f2389feade2be89 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.