Taiwan FDA registration 12d355b883bac10f14bb6f87fd20dea3
Dening Family Probiotic Pregnancy Test Pen
TW: 德甯家庭益生驗孕筆
Taiwan·Risk Class 2·Longteng Biotechnology Co., Ltd·Registered Apr 19, 2012 – Dec 12, 2015CancelledRegistration details
- Analysis ID
- 12d355b883bac10f14bb6f87fd20dea3
Company information
- Manufacturer
- Longteng Biotechnology Co., Ltd
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- DURBLIN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Qualitative detection of human chorionic gonadotropin.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 19, 2012
- Expiry Date
- Dec 12, 2015
- Cancellation Date
- Jun 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Dening Family Probiotic Pregnancy Test Pen in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12d355b883bac10f14bb6f87fd20dea3 and manufactured by Longteng Biotechnology Co., Ltd. The authorized representative in Taiwan is DURBLIN ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices