"Baxter" tissue repair coagulant spray tube
Taiwan·Risk Class 2·Clinico Medical Sp. z o.o.;; Baxter Healthcare SA·Registered May 18, 2024 – May 18, 2029Active- Analysis ID
- ab49d5d54cab5e2d17bd18c18dc86c3a
- Customs Code
- DHA05603699101
- Manufacturer Country
- Switzerland;;Poland
- Authorized Representative
- BAXTER HEALTHCARE LTD.
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5860 活塞式注射筒
- Import Information
- Input;; Contract manufacturing
- Registration Date
- May 18, 2024
- Expiry Date
- May 18, 2029
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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 ab49d5d54cab5e2d17bd18c18dc86c3a and manufactured by Clinico Medical Sp. z o.o.;; Baxter Healthcare SA. The authorized representative in Taiwan is BAXTER HEALTHCARE LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Made (部分製程) in POLAND;; Baxter Healthcare SA;; Baxter S.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.