Taiwan FDA registration ef23eac5fa779b59634063dcae5ec01a

"Intergola" surgical retractor system (non-sterile)

TW: "英特戈拉" 手術用牽開器系統 (未滅菌)

Taiwan·Risk Class 1·Integra Lifesciences Corporation·Registered Jul 16, 2024 – Jul 16, 2029Active

Registration details

Analysis ID: ef23eac5fa779b59634063dcae5ec01a
Customs Code: DHA09402354503

Company information

Manufacturer: Integra Lifesciences Corporation
Manufacturer Country: United States
Authorized Representative: ASIA-COL INTERNATIONAL CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "General Surgical Manual Instruments (I.4800)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jul 16, 2024
Expiry Date: Jul 16, 2029

About this record

Access comprehensive regulatory information for "Intergola" surgical retractor system (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ef23eac5fa779b59634063dcae5ec01a and manufactured by Integra Lifesciences Corporation. The authorized representative in Taiwan is ASIA-COL INTERNATIONAL 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.