Taiwan FDA registration 8e38deb913557ce2701a1c0ec3d96879
"Nedek" spray unit (unsterilized)
TW: “耐德克”噴霧裝置 (未滅菌)
Taiwan·Risk Class 1·NIDEK MEDICAL PRODUCTS, INC.·Registered Jun 19, 2006 – Jun 19, 2016CancelledRegistration details
- Analysis ID
- 8e38deb913557ce2701a1c0ec3d96879
- Customs Code
- DHA04400475004
Company information
- Manufacturer
- NIDEK MEDICAL PRODUCTS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- NSH MEDICAL CORP.
Product details
- Intended Use
- It is limited to the first level of identification of the "Ear, Nose and Throat Pesticide Application Device (G.5220)" of the Medical Device Management Regulations.
- 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
- Jun 19, 2006
- Expiry Date
- Jun 19, 2016
- Cancellation Date
- Jul 03, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nedek" spray unit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8e38deb913557ce2701a1c0ec3d96879 and manufactured by NIDEK MEDICAL PRODUCTS, INC.. The authorized representative in Taiwan is NSH MEDICAL CORP..
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