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"St. Riss" Ancol probe - Taiwan Registration 61d35c15b22b5f442384c2af6a3e6e18

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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61d35c15b22b5f442384c2af6a3e6e18
Registration Details
Taiwan FDA Registration: 61d35c15b22b5f442384c2af6a3e6e18
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Device Details

"St. Riss" Ancol probe
TW: “聖芮絲”安可兒探針
Risk Class 2

Registration Details

61d35c15b22b5f442384c2af6a3e6e18

DHA05603526200

Company Information

United States;;India

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1075 腸胃科-泌尿科生檢器械

import

Dates and Status

Jan 28, 2022

Jan 28, 2027