Taiwan FDA registration 6cd2474977680211b0be5641f56adf8e

"Chengwei" Madai breathing canal (unsterilized)

TW: “成威”麻醉呼吸管路 (未滅菌)

Taiwan·Risk Class 1·LILY MEDICAL CORPORATION·Registered May 15, 2006 – May 15, 2011Cancelled

Registration details

Analysis ID: 6cd2474977680211b0be5641f56adf8e

Company information

Manufacturer: LILY MEDICAL CORPORATION
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CHAIN WAVE CO., LTD.

Product details

Intended Use: It is limited to the scope of first-level identification of the "Anesthesia Breathing Pipeline (D.5240)" of the Administrative Measures for Medical Devices.
Product Type (Level 1): D Anesthesiology
Product Type (Level 2): D.5240 麻醉呼吸管路
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: May 15, 2006
Expiry Date: May 15, 2011
Cancellation Date: Apr 27, 2010

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Chengwei" Madai breathing canal (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6cd2474977680211b0be5641f56adf8e and manufactured by LILY MEDICAL CORPORATION. The authorized representative in Taiwan is CHAIN WAVE 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.