Taiwan FDA registration 07b71a9e63ccc000bfe1c68183008bad
“Reichert” iPac Pachymeter
TW: “瑞凱”艾博克角膜厚度測量儀
Taiwan·Risk Class 2·MD·REICHERT, INC.·Registered May 17, 2017 – May 17, 2027ActiveRegistration details
- Analysis ID
- 07b71a9e63ccc000bfe1c68183008bad
- License Form
- Ministry of Health Medical Device Import No. 029762
- Customs Code
- DHA05602976208
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)
- P Devices for radiology
- Product Type (Level 2)
- P1560 ultrasonic echo imaging system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 17, 2017
- Expiry Date
- May 17, 2027
About this record
Access comprehensive regulatory information for “Reichert” iPac Pachymeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 07b71a9e63ccc000bfe1c68183008bad and manufactured by REICHERT, INC.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE CO., LTD..
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