Direct total iron-binding capacity reagents for vitex biochemical products
- Analysis ID
- 5c20f5671a6ad9bf91e64adaf9a2e5ac
- Customs Code
- DHA05602683405
- Manufacturer
- ORTHO-CLINICAL DIAGNOSTICS, INC.
- Manufacturer Country
- United States
- Authorized Representative
- DKSH TAIWAN LTD.
- Intended Use
- This product needs to be used with the Vitex 5,1 FS/4600 chemical analyzer and the Vitex 5600 biochemical immunoassay analyzer to quantitatively measure the total iron-binding capacity in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1415 Iron Binding Capacity Test System;; A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products
- Import Information
- import
- Registration Date
- Dec 26, 2014
- Expiry Date
- Dec 26, 2029
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Access comprehensive regulatory information for Direct total iron-binding capacity reagents for vitex biochemical products in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5c20f5671a6ad9bf91e64adaf9a2e5ac and manufactured by ORTHO-CLINICAL DIAGNOSTICS, INC.. The authorized representative in Taiwan is DKSH TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ORTHO-CLINICAL DIAGNOSTICS, INC.;; ORTHO-CLINICAL DIAGNOSTICS, INC, 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.