Taiwan FDA registration dbca6302c570aa798fb616ac15edb197
“Reichert” Auto Tonometer
TW: “瑞凱”自動眼壓計
Taiwan·Risk Class 2·MD·REICHERT, INC.·Registered Jun 08, 2017 – Jun 08, 2022ExpiredRegistration details
- Analysis ID
- dbca6302c570aa798fb616ac15edb197
- License Form
- Ministry of Health Medical Device Import No. 029787
- Customs Code
- DHA05602978701
Company information
- Manufacturer
- REICHERT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- TAIWAN HWA IN ENTERPRISE 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
- Jun 08, 2017
- Expiry Date
- Jun 08, 2022
About this record
Access comprehensive regulatory information for “Reichert” Auto Tonometer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dbca6302c570aa798fb616ac15edb197 and manufactured by REICHERT, INC.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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