Taiwan FDA registration 389aceb827f8f8590f62febaa7c07798
"Oka Shin" Madai breathing pipeline (unsterilized)
TW: “岡新”麻醉呼吸管路（未滅菌）
Taiwan·Risk Class 1·KUNG SHIN PLASTICS CO., LTD.·Registered Aug 10, 2010 – Aug 10, 2015CancelledRegistration details
- Analysis ID
- 389aceb827f8f8590f62febaa7c07798
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 "anesthesia breathing circuit (D.5240)" of the Measures for the Administration of Medical Equipment.
- 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
- Aug 10, 2010
- Expiry Date
- Aug 10, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Oka Shin" Madai breathing pipeline (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 389aceb827f8f8590f62febaa7c07798 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