Taiwan FDA registration a60ea2bfeabe88292e275e631648e1b4

Kaiwo Technology Chlamydomydomys Test Kit (Unsterilized)

TW: 開物科技披衣菌檢測試劑盒(未滅菌)

Taiwan·Risk Class 1·SYNTRON BIORESEARCH INC.,·Registered Sep 26, 2007 – Sep 26, 2017Cancelled

Registration details

Analysis ID: a60ea2bfeabe88292e275e631648e1b4
Customs Code: DHA04400617506

Company information

Manufacturer: SYNTRON BIORESEARCH INC.,
Manufacturer Country: United States
Authorized Representative: Kaiwu Technology Co., Ltd. Tainan Branch

Product details

Intended Use: Limited to the first grade identification range of Chlamydomydia serological reagent (C.3120) for the management of medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3120 披衣菌血清試劑
Import Information: import

Dates and status

Registration Date: Sep 26, 2007
Expiry Date: Sep 26, 2017
Cancellation Date: Nov 22, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Kaiwo Technology Chlamydomydomys Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a60ea2bfeabe88292e275e631648e1b4 and manufactured by SYNTRON BIORESEARCH INC.,. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Tainan Branch.

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