Taiwan FDA registration cc91615be3011058ac6a55d2dd32a008

IMMULITE Gastrin Control

TW: 免疫特胃泌素品管液

Taiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Mar 20, 2018 – Mar 20, 2028Active

Registration details

Analysis ID: cc91615be3011058ac6a55d2dd32a008
License Form: Ministry of Health Medical Device Import No. 030528
Customs Code: DHA05603052800

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
Manufacturer Country: United Kingdom
Authorized Representative: SIEMENS HEALTHCARE LIMITED

Product details

Intended Use: This product is a double-concentration quality control solution with IMMULITE/IMMULITE 1000 and IMMULITE 2000 gastrin test reagent set for reagent quality control.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 20, 2018
Expiry Date: Mar 20, 2028

About this record

Access comprehensive regulatory information for IMMULITE Gastrin Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cc91615be3011058ac6a55d2dd32a008 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.

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