Vitex 3600 Immunodiagnostic Analyzer (Unsterilized)
Taiwan·Risk Class 1·NPA DE MEXICO S. DE R.L. DE C.V.;; ORTHO-CLINICAL DIAGNOSTICS, INC·Registered Dec 15, 2008 – Dec 15, 2023Cancelled- Analysis ID
- 153475b09b9a97c976660de5665275e0
- Customs Code
- DHA04400732109
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- DKSH TAIWAN LTD.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
- Import Information
- import
- Registration Date
- Dec 15, 2008
- Expiry Date
- Dec 15, 2023
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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Access comprehensive regulatory information for Vitex 3600 Immunodiagnostic Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 153475b09b9a97c976660de5665275e0 and manufactured by NPA DE MEXICO S. DE R.L. DE C.V.;; 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 NPA DE MEXICO S. DE R.L. DE C.V.;; 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.