"RET" Intraocular Lens Guide (Non-sterile)
Taiwan·Risk Class 1·MD·R.E.T., INC.·Registered Nov 27, 2017 – Nov 27, 2022Expired- Analysis ID
- bf3e1ba6ed9253dae5963299408436ce
- License Form
- Ministry of Health Medical Device Import No. 018549
- Customs Code
- DHA09401854904
- Manufacturer
- R.E.T., INC.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BAUSCH & LOMB TAIWAN LIMITED
- 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
- Nov 27, 2017
- Expiry Date
- Nov 27, 2022
Top companies providing products similar to ""RET" Intraocular Lens Guide (Non-sterile)"
Recently registered similar products
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 bf3e1ba6ed9253dae5963299408436ce and manufactured by R.E.T., INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RET, 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.