Taiwan FDA registration 8676c081a93447cf47ecaf21b277c23e
“Reichert” Ocular Response Analyzer
TW: “瑞凱”角膜生物力學反應分析儀
Taiwan·Risk Class 2·MD·REICHERT, INC.·Registered Dec 07, 2019 – Dec 07, 2024ExpiredRegistration details
- Analysis ID
- 8676c081a93447cf47ecaf21b277c23e
- License Form
- Ministry of Health Medical Device Import No. 033058
- Customs Code
- DHA05603305804
Company information
- Manufacturer
- REICHERT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Kang Cheng Medical Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M1930 Tonometer and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 07, 2019
- Expiry Date
- Dec 07, 2024
About this record
Access comprehensive regulatory information for “Reichert” Ocular Response Analyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8676c081a93447cf47ecaf21b277c23e and manufactured by REICHERT, INC.. The authorized representative in Taiwan is Kang Cheng Medical Technology Co., Ltd.
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