Taiwan FDA registration 36800dd4df27fdc6ee9e44f179064821

"Renzi" is poured into the filter tube group (sterilized)

TW: “仁齊”灌入過濾管組(滅菌)

Taiwan·Risk Class 1·TOP-BOUND ENTERPRISE CO., LTD.·Registered Jun 30, 2009 – Jun 30, 2014Cancelled

Registration details

Analysis ID: 36800dd4df27fdc6ee9e44f179064821

Company information

Manufacturer: TOP-BOUND ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: TOP-BOUND ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of laparoscopic perfusion device (L.1730) for the management of medical devices.
Product Type (Level 1): l Obstetrics and Gynecology
Product Type (Level 2): L.1730 腹腔鏡灌入器
Import Information: QMS/QSD;; 國產

Dates and status

Registration Date: Jun 30, 2009
Expiry Date: Jun 30, 2014
Cancellation Date: May 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Renzi" is poured into the filter tube group (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 36800dd4df27fdc6ee9e44f179064821 and manufactured by TOP-BOUND ENTERPRISE CO., LTD.. The authorized representative in Taiwan is TOP-BOUND ENTERPRISE 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.