Taiwan FDA registration 7bd9955ce8dc6a7aa1eeb96f0cf85911

"IMMUNOCATCH" Legionella (Non-Sterile)

TW: "艾美凱特" 退伍軍人肺炎尿液抗原快速診斷試劑 (未滅菌)

Taiwan·Risk Class 1·MD·EIKEN CHEMICAL CO., LTD.·Registered May 02, 2019 – May 02, 2024Expired

Registration details

Analysis ID: 7bd9955ce8dc6a7aa1eeb96f0cf85911
License Form: Ministry of Health Medical Device Import No. 020391
Customs Code: DHA09402039100

Company information

Manufacturer: EIKEN CHEMICAL CO., LTD.
Manufacturer Country: Japan
Authorized Representative: GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limit the management method of medical equipment Haemophilus serogenus (C.3300) first level identification range.
Product Type (Level 1): C Immunology and microbiology devices
Product Type (Level 2): C3300 Haemophilus serology
Import Information: Imported from abroad

Dates and status

Registration Date: May 02, 2019
Expiry Date: May 02, 2024

About this record

Access comprehensive regulatory information for "IMMUNOCATCH" Legionella (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 7bd9955ce8dc6a7aa1eeb96f0cf85911 and manufactured by EIKEN CHEMICAL CO., LTD.. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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