Taiwan FDA registration 5d87a9d5529119717b87f94979aefd83
"Schiller" Magraft standard physiological monitoring equipment
TW: “席勒”美格萊富標準型生理監視設備
Taiwan·Risk Class 2·SCHILLER MEDICAL·Registered Jun 30, 2010 – Jun 30, 2020CancelledRegistration details
- Analysis ID
- 5d87a9d5529119717b87f94979aefd83
- Customs Code
- DHA00602117703
Company information
- Manufacturer
- SCHILLER MEDICAL
- Manufacturer Country
- France
- Authorized Representative
- GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH
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.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2010
- Expiry Date
- Jun 30, 2020
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Schiller" Magraft standard physiological monitoring equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5d87a9d5529119717b87f94979aefd83 and manufactured by SCHILLER MEDICAL. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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