Taiwan FDA registration 4e423cff80a54a081fece2e29e68fb15

Longteng ovulation in vitro reagent card

TW: 龍騰排卵體外試劑卡

Taiwan·Risk Class 1·Longteng Biotechnology Co., Ltd·Registered May 08, 2006 – May 08, 2011Cancelled

Registration details

Analysis ID: 4e423cff80a54a081fece2e29e68fb15
Customs Code: DHY04300134502

Company information

Manufacturer: Longteng Biotechnology Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Longteng Biotechnology Co., Ltd

Product details

Intended Use: It is used to detect the impotence of xanthopoietin (LH) in human urine.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1485 Progesterone testing system
Import Information: import

Dates and status

Registration Date: May 08, 2006
Expiry Date: May 08, 2011
Cancellation Date: Nov 05, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Longteng ovulation in vitro reagent card in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4e423cff80a54a081fece2e29e68fb15 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is Longteng Biotechnology Co., Ltd.

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