Taiwan FDA registration 38c90eca11b6ead78fdbe1be5361d0af
"Di Cheng" respirator tubing (unsterilized)
TW: “狄成”呼吸器管路（未滅菌）
Taiwan·Risk Class 1·DI CHENG RUBBER INDUSTRIES INC.·Registered Apr 06, 2009 – Apr 06, 2024ExpiredRegistration details
- Analysis ID
- 38c90eca11b6ead78fdbe1be5361d0af
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 range of the "Respirator Pipeline (D.5975)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5975 Respirator Tubing
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 06, 2009
- Expiry Date
- Apr 06, 2024
About this record
Access comprehensive regulatory information for "Di Cheng" respirator tubing (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 38c90eca11b6ead78fdbe1be5361d0af and manufactured by DI CHENG RUBBER INDUSTRIES INC.. The authorized representative in Taiwan is DI CHENG RUBBER INDUSTRIES INC..
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