Taiwan FDA registration 75c50b37ca6f0e4b9e741da06df1bcc1

"Cosmo" Endoscope Warmer (Sterile)

TW: "禾祺銳" 內視鏡加溫包 (滅菌)

Taiwan·Risk Class 1·MD·COSMO BIOTECH CO., LTD.·Registered Mar 27, 2017 – Mar 27, 2022Cancelled

Registration details

Analysis ID: 75c50b37ca6f0e4b9e741da06df1bcc1
License Form: Ministry of Health Medical Device Manufacturing No. 006659

Company information

Manufacturer: COSMO BIOTECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: COSMO BIOTECH CO., LTD.

Product details

Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H1500 endoscope and accessories
Import Information: Produced in Taiwan, China; GMP

Dates and status

Registration Date: Mar 27, 2017
Expiry Date: Mar 27, 2022
Cancellation Date: Jan 11, 2022

Cancellation information

Status: Logged out
Reason: 自請註銷

About this record

Access comprehensive regulatory information for "Cosmo" Endoscope Warmer (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 75c50b37ca6f0e4b9e741da06df1bcc1 and manufactured by COSMO BIOTECH CO., LTD.. The authorized representative in Taiwan is COSMO 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.