Taiwan FDA registration 571ab8323857ffe70cc7fa976787577e
"Lady Kang" cervical dilator stick (sterilized)
TW: "女康" 子宮頸擴張棒 (滅菌)
Taiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Sep 27, 2022 – Sep 27, 2027ActiveRegistration details
- Analysis ID
- 571ab8323857ffe70cc7fa976787577e
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PACIFIC HOSPITAL SUPPLY CO., LTD.
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
- Sep 27, 2022
- Expiry Date
- Sep 27, 2027
About this record
Access comprehensive regulatory information for "Lady Kang" cervical dilator stick (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 571ab8323857ffe70cc7fa976787577e and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY CO., LTD..
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