Taiwan FDA registration 2571d0ebd5c5e5be559991d2e1177324
"Kitajiko" uterine contraceptive remover (sterilization)
TW: "北極光" 子宮內避孕器去除器(滅菌)
Taiwan·Risk Class 1·Northern Lights Industrial Co., Ltd. Dongshi Factory·Registered Mar 11, 2024 – Mar 11, 2029ActiveRegistration details
- Analysis ID
- 2571d0ebd5c5e5be559991d2e1177324
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Northern Lights Industrial Co., Ltd. Dongshi Factory
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "manual instruments for obstetrics and gynecology (L.4530)" the first level identification range.
- Product Type (Level 1)
- l Obstetrics and Gynecology
- Product Type (Level 2)
- L.4530 婦產科專用手動器械
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Mar 11, 2024
- Expiry Date
- Mar 11, 2029
About this record
Access comprehensive regulatory information for "Kitajiko" uterine contraceptive remover (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2571d0ebd5c5e5be559991d2e1177324 and manufactured by Northern Lights Industrial Co., Ltd. Dongshi Factory. The authorized representative in Taiwan is Northern Lights Industrial Co., Ltd. Dongshi Factory.
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