Taiwan FDA registration 61d35c15b22b5f442384c2af6a3e6e18
"St. Riss" Ancol probe
TW: “聖芮絲”安可兒探針
Taiwan·Risk Class 2·Made (部分製程) in INDIA;; SenoRx, Inc.·Registered Jan 28, 2022 – Jan 28, 2027ActiveRegistration details
- Analysis ID
- 61d35c15b22b5f442384c2af6a3e6e18
- Customs Code
- DHA05603526200
Company information
- Manufacturer
- Made (部分製程) in INDIA;; SenoRx, Inc.
- Manufacturer Country
- United States;;India
- Authorized Representative
- BARD PACIFIC HEALTH CARE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Jan 28, 2022
- Expiry Date
- Jan 28, 2027
About this record
Access comprehensive regulatory information for "St. Riss" Ancol probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 61d35c15b22b5f442384c2af6a3e6e18 and manufactured by Made (部分製程) in INDIA;; SenoRx, Inc.. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..
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