Taiwan FDA registration 1fed515dc4cfedd9033b6c0adab43e95
"Acikang" Maimaton breast biopsy system
TW: “愛惜康”麥瑪通乳房活體組織切片檢查系統
Taiwan·Risk Class 2·ETHICON ENDO-SURGERY, INC.·Registered Feb 25, 2008 – Feb 25, 2013CancelledRegistration details
- Analysis ID
- 1fed515dc4cfedd9033b6c0adab43e95
- Customs Code
- DHA00601861201
Company information
- Manufacturer
- ETHICON ENDO-SURGERY, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Defeng Technology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.1075 腸胃科-泌尿科生檢器械
- Import Information
- import
Dates and status
- Registration Date
- Feb 25, 2008
- Expiry Date
- Feb 25, 2013
- Cancellation Date
- Jun 17, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Acikang" Maimaton breast biopsy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1fed515dc4cfedd9033b6c0adab43e95 and manufactured by ETHICON ENDO-SURGERY, INC.. The authorized representative in Taiwan is Defeng Technology Co., Ltd.
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