Taiwan FDA registration 6cf8113c94ec9beb6a44921b37fb4ba7

Medical trial beauty portable ovulation pregnancy test detection recorder

TW: 醫試美攜帶式排卵驗孕偵測紀錄器

Taiwan·Risk Class 2·Kaiwu Technology Co., Ltd. Nanke Factory·Registered Aug 01, 2018 – Aug 01, 2028Active

Registration details

Analysis ID: 6cf8113c94ec9beb6a44921b37fb4ba7

Company information

Manufacturer: Kaiwu Technology Co., Ltd. Nanke Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Kaiwu Technology Co., Ltd. Nanke Factory

Product details

Intended Use: This product can be used with a medical aesthetic ovulation rapid test pen to semi-quantitatively detect LH (luteinizing hormone) in urine, and a medical beauty pregnancy rapid test pen can qualitatively test hCG (human chorionic gonadotropin) in urine. This product is intended for use by professionals and general personnel.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1155 Human chorionic gonadotropin testing system;; A.1485 Progesterone testing system
Import Information: Domestic

Dates and status

Registration Date: Aug 01, 2018
Expiry Date: Aug 01, 2028

About this record

Access comprehensive regulatory information for Medical trial beauty portable ovulation pregnancy test detection recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6cf8113c94ec9beb6a44921b37fb4ba7 and manufactured by Kaiwu Technology Co., Ltd. Nanke Factory. The authorized representative in Taiwan is Kaiwu Technology Co., Ltd. Nanke Factory.

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