Taiwan FDA registration a40281a3d019696899398a489d8ead19
"Pacific" closed suction sleeve (sterilized)
TW: “太平洋”密閉式抽痰套 (滅菌)
Taiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Jul 11, 2006 – Jul 11, 2026ExpiredRegistration details
- Analysis ID
- a40281a3d019696899398a489d8ead19
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 method of medical equipment, tracheobronchial suction catheter (D.6810) first level identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube
- Import Information
- QMS/QSD;; 國產
Dates and status
- Registration Date
- Jul 11, 2006
- Expiry Date
- Jul 11, 2026
About this record
Access comprehensive regulatory information for "Pacific" closed suction sleeve (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a40281a3d019696899398a489d8ead19 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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