Taiwan FDA registration c1e73c1a72735e42c786c470520680ec

"Create Biotech" Tracheal Tube Fixation Device (Non-Sterile)

TW: "佳創" 氣管管路固定裝置 (未滅菌)

Taiwan·Risk Class 1·MD·Longtan Factory of Jiachuang Biotechnology Co., Ltd·Registered May 17, 2019 – May 17, 2024Expired

Registration details

Analysis ID: c1e73c1a72735e42c786c470520680ec
License Form: Ministry of Health Medical Device Manufacturing No. 007767

Company information

Manufacturer: Longtan Factory of Jiachuang Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CREATE BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5770 Tracheal Line Fixture
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: May 17, 2019
Expiry Date: May 17, 2024

About this record

Access comprehensive regulatory information for "Create Biotech" Tracheal Tube Fixation Device (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 c1e73c1a72735e42c786c470520680ec and manufactured by Longtan Factory of Jiachuang Biotechnology Co., Ltd. The authorized representative in Taiwan is CREATE BIOTECH 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.