Taiwan FDA registration 1ff32fffee7a0cdb1a4546f94b81082d
“NEILMED” Sinus Rinse Regular Kit (Non-sterile)
TW: “耐有美”賽那靈洗鼻器 (未滅菌)
Taiwan·Risk Class 1·MD·NEILMED PHARMACEUTICALS, INC.·Registered Jan 28, 2014 – Jan 28, 2019CancelledRegistration details
- Analysis ID
- 1ff32fffee7a0cdb1a4546f94b81082d
- License Form
- Ministry of Health Medical Device Import No. 013823
- Customs Code
- DHA09401382302
Company information
- Manufacturer
- NEILMED PHARMACEUTICALS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ENTMED CO., LTD.
Product details
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G5220 ENT dosing device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 28, 2014
- Expiry Date
- Jan 28, 2019
- Cancellation Date
- Dec 24, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “NEILMED” Sinus Rinse Regular Kit (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 1ff32fffee7a0cdb1a4546f94b81082d and manufactured by NEILMED PHARMACEUTICALS, INC.. The authorized representative in Taiwan is ENTMED CO., LTD..
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