Taiwan FDA registration ec822126fec1883e22f5cbb44e48d718
"Oka Shin" Madai breathing canal (unsterilized)
TW: "岡新" 麻醉呼吸管路 (未滅菌)
Registration details
- Analysis ID
- ec822126fec1883e22f5cbb44e48d718
Company information
- Manufacturer
- KUNG SHIN PLASTICS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- KUNG SHIN PLASTICS CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the classification and grading management measures for medical equipment "anesthesia breathing circuit (D.5240)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5240 麻醉呼吸管路
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 08, 2015
- Expiry Date
- Dec 08, 2025
About this record
Access comprehensive regulatory information for "Oka Shin" 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 ec822126fec1883e22f5cbb44e48d718 and manufactured by KUNG SHIN PLASTICS CO., LTD.. The authorized representative in Taiwan is KUNG SHIN PLASTICS 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.
Free DatabasePowered by Pure Global AI89,000+ Devices