Taiwan FDA registration 380d0e3b3da9f7fae5f3e298bacbe594
"Dicheng" pressure line and its accessories (unsterilized)
TW: “狄成”壓力管路及其附件(未滅菌)
Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Apr 06, 2009 – Apr 06, 2024ExpiredRegistration details
- Analysis ID
- 380d0e3b3da9f7fae5f3e298bacbe594
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
- Limited to the first level identification scope of pressure pipelines and their accessories (D.5860) of the classification and grading management measures for medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5860 Pressure lines and accessories thereof
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 06, 2009
- Expiry Date
- Apr 06, 2024
About this record
Access comprehensive regulatory information for "Dicheng" pressure line and its accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 380d0e3b3da9f7fae5f3e298bacbe594 and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices