Taiwan FDA registration 504f1ff904d9c0bacca6482e3936c6af

"Nofaferri" Legionnaires' Disease Test Set (Unsterilized)

TW: "諾法鐵" 退伍軍人症檢驗試劑組 (未滅菌)

Taiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered Nov 16, 2017 – Nov 16, 2027Active

Registration details

Analysis ID: 504f1ff904d9c0bacca6482e3936c6af
Customs Code: DHA09401851500

Company information

Manufacturer: GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH
Manufacturer Country: Germany
Authorized Representative: EVERLIGHT BIOTECH(TAIWAN) CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of Haemophilus serum reagent (C.3300) in the classification and grading management method of medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3300 嗜血桿菌屬血清試劑
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Nov 16, 2017
Expiry Date: Nov 16, 2027

About this record

Access comprehensive regulatory information for "Nofaferri" Legionnaires' Disease Test Set (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 504f1ff904d9c0bacca6482e3936c6af and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..

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