Taiwan FDA registration e9f1b54b8f2391d482c2ad096290342b

"Siemens Atellica" Magnesium (MG) test (Non-Sterile)

TW: "西門子"鎂試劑 (未滅菌)

Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LIMITED·Registered Sep 11, 2017 – Sep 11, 2027Active

Registration details

Analysis ID: e9f1b54b8f2391d482c2ad096290342b
License Form: Ministry of Health Medical Device Import No. 018294
Customs Code: DHA09401829400

Company information

Manufacturer: RANDOX LABORATORIES LIMITED
Manufacturer Country: United Kingdom
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: Limited to the first level identification range of the "Magnesium Test System (A.1495)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1495 Magnesium Test System
Import Information: Imported from abroad

Dates and status

Registration Date: Sep 11, 2017
Expiry Date: Sep 11, 2027

About this record

Access comprehensive regulatory information for "Siemens Atellica" Magnesium (MG) test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e9f1b54b8f2391d482c2ad096290342b and manufactured by RANDOX LABORATORIES LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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