Taiwan FDA registration 5d73d55867aecc54e5254d7279b13363
"E-GMED" Tracheal Tube Fixation Device (Non-Sterile)
TW: "醫技" 氣管管路固定裝置 (未滅菌)
Taiwan·Risk Class 1·MD·E-GMED HEALTH CO., LTD·Registered Nov 10, 2016 – Nov 10, 2026ActiveRegistration details
- Analysis ID
- 5d73d55867aecc54e5254d7279b13363
- License Form
- Ministry of Health Medical Device Manufacturing No. 006461
Company information
- Manufacturer
- E-GMED HEALTH CO., LTD
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- E-GMED HEALTH CO., LTD
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Tracheal Pipeline Fixation Device (D.5770)".
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5770 Tracheal Line Fixture
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 10, 2016
- Expiry Date
- Nov 10, 2026
About this record
Access comprehensive regulatory information for "E-GMED" Tracheal Tube Fixation Device (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 5d73d55867aecc54e5254d7279b13363 and manufactured by E-GMED HEALTH CO., LTD. The authorized representative in Taiwan is E-GMED HEALTH CO., LTD.
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