Taiwan FDA registration f4525b68b509ea4d42fdc4796db25341
"Pacific" Closed Suction Tube Pack (Sterilized)
TW: "太平洋" 密閉式抽痰管包 (滅菌)
Taiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Dec 14, 2016 – Dec 14, 2026ActiveRegistration details
- Analysis ID
- f4525b68b509ea4d42fdc4796db25341
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PACIFIC HOSPITAL SUPPLY CO., LTD.
Product details
- Intended Use
- By providing the suction power with an external vacuum source, liquid or semi-solid is extracted from the patient's upper respiratory tract (some models have MDI dosing ports for the purpose of administering the patient), the following blanks.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.9999 Miscellaneous
- Import Information
- 國產;; QMS/QSD
Dates and status
- Registration Date
- Dec 14, 2016
- Expiry Date
- Dec 14, 2026
About this record
Access comprehensive regulatory information for "Pacific" Closed Suction Tube Pack (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f4525b68b509ea4d42fdc4796db25341 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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