Taiwan FDA registration d53b6a57a5402d1425561fca4b41c744
"Dage" throat mask (unsterilized)
TW: “達吉”喉頭面罩 (未滅菌)
Registration details
- Analysis ID
- d53b6a57a5402d1425561fca4b41c744
- Customs Code
- DHA04400589407
Company information
- Manufacturer
- THE LARYNGEAL MASK COMPANY LIMITED
- Manufacturer Country
- Seychelles
- Authorized Representative
- BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- import
Dates and status
- Registration Date
- May 21, 2007
- Expiry Date
- May 21, 2017
- Cancellation Date
- Dec 13, 2019
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Dage" throat mask (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d53b6a57a5402d1425561fca4b41c744 and manufactured by THE LARYNGEAL MASK COMPANY LIMITED. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE 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