"RET" Intraocular Lens Guide (Non-Sterile)
- Analysis ID
- 93137ca76767043ed0547fcec6edab60
- License Form
- Ministry of Health Medical Device Import No. 017755
- Customs Code
- DHA09401775502
- Manufacturer
- RET, INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- ICARES MEDICUS, INC.
- Intended Use
- Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M4300 Intraocular Lens Guide
- Import Information
- Imported from abroad
- Registration Date
- Apr 24, 2017
- Expiry Date
- Apr 24, 2022
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Access comprehensive regulatory information for "RET" Intraocular Lens Guide (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 93137ca76767043ed0547fcec6edab60 and manufactured by RET, INC.. The authorized representative in Taiwan is ICARES MEDICUS, INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including R.E.T., 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.