Taiwan FDA registration e42f5bb78eeaf3345f02023a5fe46b15

"Emti" laparoscopic gas filter tube (sterilization)

TW: "愛姆提" 腹腔鏡氣體過濾管器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·MTP MEDICAL TECHNICAL PROMOTION GMBH·Registered Feb 05, 2015 – Feb 05, 2020Cancelled
Registration details
Analysis ID
e42f5bb78eeaf3345f02023a5fe46b15
Customs Code
DHA09401490200
Company information
Manufacturer Country
Germany
Authorized Representative
Huixing 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
Input;; QMS/QSD
Dates and status
Registration Date
Feb 05, 2015
Expiry Date
Feb 05, 2020
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
About this record

Access comprehensive regulatory information for "Emti" laparoscopic gas filter tube (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e42f5bb78eeaf3345f02023a5fe46b15 and manufactured by MTP MEDICAL TECHNICAL PROMOTION GMBH. The authorized representative in Taiwan is Huixing 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.

Free DatabasePowered by Pure Global AI89,000+ Devices