Taiwan FDA registration 4280899ce480a7e50d1f39f7c6ae291b
"Merotek" Nevix movable catheter
TW: “麥洛泰克”奈維克斯活動式導管
Taiwan·Risk Class 2·MYELOTEC, INC.·Registered Jul 27, 2012 – Jul 27, 2022CancelledRegistration details
- Analysis ID
- 4280899ce480a7e50d1f39f7c6ae291b
- Customs Code
- DHA00602391000
Company information
- Manufacturer
- MYELOTEC, INC.
- Manufacturer Country
- United States
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5120 麻醉傳輸導管
- Import Information
- import
Dates and status
- Registration Date
- Jul 27, 2012
- Expiry Date
- Jul 27, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Merotek" Nevix movable catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4280899ce480a7e50d1f39f7c6ae291b and manufactured by MYELOTEC, INC.. The authorized representative in Taiwan is REVO LASER CORPORATION.
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