"Tongda" pressure regulator (unsterilized)
Taiwan·Risk Class 1·Zhongli Technology Co., Ltd. Factory 2;; Tongda Instrument Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2022Cancelled- Analysis ID
- d582f30c56bcf743ba175be2fbf70811
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- RESPTECH CO., LTD.
- Intended Use
- Limited to the first level identification range of the pressure regulator (D.2700) of the management method for medical equipment.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.2700 Pressure Regulator
- Import Information
- 國產;; 委託製造;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2022
- Cancellation Date
- Feb 01, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Tongda" pressure regulator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d582f30c56bcf743ba175be2fbf70811 and manufactured by Zhongli Technology Co., Ltd. Factory 2;; Tongda Instrument Co., Ltd. The authorized representative in Taiwan is RESPTECH CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including The second factory of Zhongli Technology Co., Ltd, and 1 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.