"Rheinland" manual eye surgery instruments
Taiwan·Risk Class 1·RHEIN MEDICAL INC.·Registered Apr 26, 2006 – Apr 26, 2011Cancelled- Analysis ID
- 0e2ccdc732c4a1661027cfc84f77250c
- Customs Code
- DHA04400423705
- Manufacturer
- RHEIN MEDICAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- FEDERAL MEDICAL CO., LTD.
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.4350 手動式眼科手術器械
- Import Information
- import
- Registration Date
- Apr 26, 2006
- Expiry Date
- Apr 26, 2011
- Cancellation Date
- Nov 26, 2012
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Rheinland" manual eye surgery instruments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e2ccdc732c4a1661027cfc84f77250c and manufactured by RHEIN MEDICAL INC.. The authorized representative in Taiwan is FEDERAL MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RHEIN MEDICAL 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.