"Baxter" tissue repair coagulant spray tube
Taiwan·Risk Class 2·Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.·Registered Feb 01, 2008 – Feb 01, 2028Active- Analysis ID
- fa04901ca763acc0c9e8a697eabad256
- Customs Code
- DHA00601857607
- Manufacturer Country
- Belgium;;Switzerland;;Poland
- Authorized Representative
- BAXTER HEALTHCARE LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
- Registration Date
- Feb 01, 2008
- Expiry Date
- Feb 01, 2028
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Access comprehensive regulatory information for "Baxter" tissue repair coagulant spray tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa04901ca763acc0c9e8a697eabad256 and manufactured by Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.A.. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Clinico Medical Sp. z o.o.;; Baxter Healthcare SA, 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.