Taiwan FDA registration 477c0d83c6995c303fc22a9a1a290344
"Schiller" Argus patient monitor
TW: “席勒”亞格斯病患監視器
Taiwan·Risk Class 3·SCHILLER AG·Registered Jul 22, 2011 – Jul 22, 2016CancelledRegistration details
- Analysis ID
- 477c0d83c6995c303fc22a9a1a290344
- Customs Code
- DHA00602248700
Company information
- Manufacturer
- SCHILLER AG
- Manufacturer Country
- Switzerland
- 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.5310 自動體外去顫器系統
- Import Information
- import
Dates and status
- Registration Date
- Jul 22, 2011
- Expiry Date
- Jul 22, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Schiller" Argus patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 477c0d83c6995c303fc22a9a1a290344 and manufactured by SCHILLER AG. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.
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