Taiwan FDA registration 88f2cab4cf0d28fbd3818365e29f190f
"Di Cheng" nasal oxygen catheter (unsterilized)
TW: "狄成" 經鼻氧氣導管 (未滅菌)
Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Dec 18, 2013 – Dec 18, 2023ExpiredRegistration details
- Analysis ID
- 88f2cab4cf0d28fbd3818365e29f190f
Company information
- Manufacturer
- DI CHENG RUBBER INDUSTRIES INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DI CHENG RUBBER INDUSTRIES INC.
Product details
- Intended Use
- It is limited to the first level of identification scope of the "Nasal Oxygen Catheter (D.5350)" of the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5350 Nasal oxygen catheters
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 18, 2013
- Expiry Date
- Dec 18, 2023
About this record
Access comprehensive regulatory information for "Di Cheng" nasal oxygen catheter (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 88f2cab4cf0d28fbd3818365e29f190f and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..
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