Taiwan FDA registration d32281954a796b616c9321c9d75b7a44

Zhongli pressure regulator (unsterilized)

TW: “眾里”壓力調節器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·The second factory of Zhongli Technology Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
d32281954a796b616c9321c9d75b7a44
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
ACARE TECHNOLOGY CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "pressure regulator (D.2700)" of the classification and grading management method for medical equipment.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.2700 Pressure Regulator
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for Zhongli 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 d32281954a796b616c9321c9d75b7a44 and manufactured by The second factory of Zhongli Technology Co., Ltd. The authorized representative in Taiwan is ACARE TECHNOLOGY 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.

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