Taiwan FDA registration 0f2581a5c3e02f6462e1aae7c0a2f907
"Genari" pulse oximeter
TW: “杰納瑞”脈搏血氧濃度計
Taiwan·Risk Class 2·General Meditech, Inc·Registered Feb 13, 2014 – Feb 13, 2019CancelledRegistration details
- Analysis ID
- 0f2581a5c3e02f6462e1aae7c0a2f907
- Customs Code
- DHA09200057508
Company information
- Manufacturer
- General Meditech, Inc
- Manufacturer Country
- China
- Authorized Representative
- SCHMIDT SCIENTIFIC TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2700.
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Feb 13, 2014
- Expiry Date
- Feb 13, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Genari" pulse oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f2581a5c3e02f6462e1aae7c0a2f907 and manufactured by General Meditech, Inc. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..
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