Taiwan FDA registration e077d494b656ab4d761c88243400c343
"AOK" Anesthesia Breathing Circuit (Non-Sterile)
TW: "飛速" 麻醉呼吸管路 (未滅菌)
Taiwan·Risk Class 1·MD·AOK TOOLING LTD·Registered Aug 03, 2015 – Aug 03, 2020CancelledRegistration details
- Analysis ID
- e077d494b656ab4d761c88243400c343
- License Form
- Ministry of Health Medical Device Land Transport No. 002468
- Customs Code
- DHA09600246800
Company information
- Manufacturer
- AOK TOOLING LTD
- Manufacturer Country
- China
- Authorized Representative
- AOK MEDTECH INC.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5240 Anesthesia breathing line
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Aug 03, 2015
- Expiry Date
- Aug 03, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "AOK" Anesthesia Breathing Circuit (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 e077d494b656ab4d761c88243400c343 and manufactured by AOK TOOLING LTD. The authorized representative in Taiwan is AOK MEDTECH INC..
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