"Pacific" Sputum Collector (Sterilization)
Taiwan·Risk Class 1·Pacific Medical Materials Co., Ltd. Copper Factory·Registered Mar 06, 2014 – Mar 06, 2029Active- Analysis ID
- 2bac6e78eb9e557711e19747bdd33b73
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PACIFIC HOSPITAL SUPPLY CO., LTD.
- Intended Use
- It is limited to the first level of identification of the "Tracheobronchial Suction Catheter (D.6810)" and "Microbial Sample Collection and Transport Equipment (C.2900)" of the Classification and Grading Management Measures for Medical Devices.
- Product Type (Level 1)
- D 麻醉科學;; C 免疫學及微生物學
- Product Type (Level 2)
- D.6810 Pneumatic bronchial suction guide tube;; C.2900 Microbial sample collection and delivery equipment
- Import Information
- 國產;; QMS/QSD
- Registration Date
- Mar 06, 2014
- Expiry Date
- Mar 06, 2029
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Access comprehensive regulatory information for "Pacific" Sputum Collector (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2bac6e78eb9e557711e19747bdd33b73 and manufactured by Pacific Medical Materials Co., Ltd. Copper Factory. The authorized representative in Taiwan is PACIFIC HOSPITAL SUPPLY CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Pacific Medical Materials Co., Ltd. Copper Factory, and 2 recent registrations in the same category. 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.