Taiwan FDA registration 247ffa60afa30d086b539e231f40a280

"YIKA" Nasal Oxygen Cannula (Non-Sterile)

TW: "宜康" 經鼻氧氣套管(未滅菌)

Taiwan·Risk Class 1·MD·YIKA MEDICAL CO., LTD.·Registered Jan 14, 2020 – Jan 14, 2025Expired

Registration details

Analysis ID: 247ffa60afa30d086b539e231f40a280
License Form: Ministry of Health Medical Device Manufacturing No. 008138

Company information

Manufacturer: YIKA MEDICAL CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: YIKA MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Nasal Oxygen Cannula (D.5340)".
Product Type (Level 1): D Devices for anesthesiology
Product Type (Level 2): D5340 Transnasal oxygen cannula
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jan 14, 2020
Expiry Date: Jan 14, 2025

About this record

Access comprehensive regulatory information for "YIKA" Nasal Oxygen Cannula (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 247ffa60afa30d086b539e231f40a280 and manufactured by YIKA MEDICAL CO., LTD.. The authorized representative in Taiwan is YIKA MEDICAL 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.