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"Siemens" Reference Solution Kit (for Confirmation Enzyme Immunoassay Analyzer) (Unsterilized) - Taiwan Registration 797160aa2cca4eaf50ac8b0520c39aba

Access comprehensive regulatory information for "Siemens" Reference Solution Kit (for Confirmation Enzyme Immunoassay 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 797160aa2cca4eaf50ac8b0520c39aba and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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797160aa2cca4eaf50ac8b0520c39aba
Registration Details
Taiwan FDA Registration: 797160aa2cca4eaf50ac8b0520c39aba
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Device Details

"Siemens" Reference Solution Kit (for Confirmation Enzyme Immunoassay Analyzer) (Unsterilized)
TW: โ€œ่ฅฟ้–€ๅญโ€ๅƒ่€ƒๆบถๆถฒ่ฉฆๅŠ‘็ต„ (็”จๆ–ผ็ขบ่ช้…ต็ด ๅ…็–ซๅˆ†ๆžๅ„€)๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

797160aa2cca4eaf50ac8b0520c39aba

DHA04400919603

Company Information

Product Details

Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1660 Quality control materials (analytical and non-analytical)

import

Dates and Status

Sep 15, 2010

Sep 15, 2020

Feb 09, 2021

Cancellation Information

Logged out

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