Taiwan FDA registration 82d29035adb1c3e7461bd279d9940cb2

"EUROIMMUN" IIFT: Stomach (Monkey)

TW: "歐蒙"免疫螢光法抗胃壁細胞抗體檢測試劑

Taiwan·Risk Class 2·MD·EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG·Registered Mar 27, 2020 – Mar 27, 2025Expired

Registration details

Analysis ID: 82d29035adb1c3e7461bd279d9940cb2
License Form: Ministry of Health Medical Device Import No. 033462
Customs Code: DHA05603346201

Company information

Manufacturer: EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG
Manufacturer Country: Germany
Authorized Representative: EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE)

Product details

Intended Use: This kit is used for in vitro qualitative or semi-quantitative detection of anti-parietal cell antibody immunoglobulin G (IgG) in patient samples.
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C5660 Multiple autologous antibody immunoassay system
Import Information: Imported from abroad

Dates and status

Registration Date: Mar 27, 2020
Expiry Date: Mar 27, 2025

About this record

Access comprehensive regulatory information for "EUROIMMUN" IIFT: Stomach (Monkey) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82d29035adb1c3e7461bd279d9940cb2 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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