Taiwan FDA registration 7b9f246c31b671bf4de65debc0472cac
"Taimu" Andobec coronary endothelial dysfunction auxiliary diagnostic device
TW: “泰姆”安多培冠狀動脈內皮功能障礙輔助診斷設備
Taiwan·Risk Class 2·ITAMAR MEDICAL LTD.·Registered Mar 12, 2010 – Mar 12, 2015CancelledRegistration details
- Analysis ID
- 7b9f246c31b671bf4de65debc0472cac
- Customs Code
- DHA00602070204
Company information
- Manufacturer
- ITAMAR MEDICAL LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- MEDICARE UNITECH INC.
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.1425 Programmable diagnostic computer
- Import Information
- import
Dates and status
- Registration Date
- Mar 12, 2010
- Expiry Date
- Mar 12, 2015
- Cancellation Date
- Jun 08, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Taimu" Andobec coronary endothelial dysfunction auxiliary diagnostic device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7b9f246c31b671bf4de65debc0472cac and manufactured by ITAMAR MEDICAL LTD.. The authorized representative in Taiwan is MEDICARE UNITECH INC..
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