"Baxter" Effluent Collection Bag (Sterilization)
Taiwan·Risk Class 1·GAMBRO DASCO S.p.A.; Made (部分製程) in SLOVENIA·Registered Nov 15, 2019 – Nov 15, 2029Active- Analysis ID
- 4c6475453a71a497385b1193e6757b0d
- Customs Code
- DHA09402101707
- Manufacturer
- GAMBRO DASCO S.p.A.; Made (部分製程) in SLOVENIA
- Manufacturer Country
- Italy;;Slovenia
- Authorized Representative
- BAXTER HEALTHCARE LTD.
- Intended Use
- It is limited to the scope of the first level of identification of the "Hemodialysis System and Its Accessories (H.5820)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Nov 15, 2019
- Expiry Date
- Nov 15, 2029
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Access comprehensive regulatory information for "Baxter" Effluent Collection Bag (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4c6475453a71a497385b1193e6757b0d and manufactured by GAMBRO DASCO S.p.A.; Made (部分製程) in SLOVENIA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Baxter Limited;; GAMBRO DASCO S.p.A., and 1 recent registrations in the same category. 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.