Taiwan FDA registration 4e791f218433490e50d0ddd9a74e71c0
"Belle" neti wash (unsterilized)
TW: “貝兒法”洗鼻器 (未滅菌)
Taiwan·Risk Class 1·BIOPHA LABORATORIES·Registered Sep 25, 2008 – Sep 25, 2013CancelledRegistration details
- Analysis ID
- 4e791f218433490e50d0ddd9a74e71c0
- Customs Code
- DHA04400709602
Company information
- Manufacturer
- BIOPHA LABORATORIES
- Manufacturer Country
- France
- Authorized Representative
- BRIGHT TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "ENT Dispensing Devices (G.5220)".
- Product Type (Level 1)
- G ENT Science
- Product Type (Level 2)
- G.5220 Ear, nose and throat applicators and substances used in conjunction thereof
- Import Information
- import
Dates and status
- Registration Date
- Sep 25, 2008
- Expiry Date
- Sep 25, 2013
- Cancellation Date
- Aug 13, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Belle" neti wash (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e791f218433490e50d0ddd9a74e71c0 and manufactured by BIOPHA LABORATORIES. The authorized representative in Taiwan is BRIGHT TRADING 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