Taiwan FDA registration ecc15adcf17c400a5b4002fab295c4a7
"I-Gel" LARYNGEAL MASK AIRWAY (Non-Sterile)
TW: "艾捷" 喉頭面罩 (未滅菌)
Taiwan·Risk Class 1·MD·INTERSURGICAL LTD.·Registered Jul 19, 2017 – Jul 19, 2022CancelledRegistration details
- Analysis ID
- ecc15adcf17c400a5b4002fab295c4a7
- License Form
- Ministry of Health Medical Device Import No. 018085
- Customs Code
- DHA09401808501
Company information
- Manufacturer
- INTERSURGICAL LTD.
- Manufacturer Country
- Lithuania
- Authorized Representative
- FU SHING MEDICAL CO., LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5110 Oropharyngeal airway tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 19, 2017
- Expiry Date
- Jul 19, 2022
- Cancellation Date
- Dec 24, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "I-Gel" LARYNGEAL MASK AIRWAY (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 ecc15adcf17c400a5b4002fab295c4a7 and manufactured by INTERSURGICAL LTD.. The authorized representative in Taiwan is FU SHING 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.
Free DatabasePowered by Pure Global AI89,000+ Devices