Taiwan FDA registration ce0cc7370c98abe5805524cb3bae9065

"Side" Helicobacter pylori antigen rapid test kit

TW: “司德”幽門螺旋桿菌抗原快速檢測試劑套組

Taiwan·Risk Class 1·STANDARD DIAGNOSTICS, INC.·Registered Dec 02, 2009 – Dec 02, 2014Cancelled

Registration details

Analysis ID: ce0cc7370c98abe5805524cb3bae9065
Customs Code: DHA04400835505

Company information

Manufacturer: STANDARD DIAGNOSTICS, INC.
Manufacturer Country: Korea, Republic of
Authorized Representative: LINKSEAS TRADING CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Helicobacter Serological Reagent (C.0003)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.0003 螺旋桿菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Dec 02, 2009
Expiry Date: Dec 02, 2014
Cancellation Date: May 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Side" Helicobacter pylori antigen rapid test kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ce0cc7370c98abe5805524cb3bae9065 and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is LINKSEAS TRADING CO., LTD..

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