Taiwan FDA registration 439513c375110047c8756bda884127ba

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 Aug 17, 2010 – Aug 17, 2025Cancelled
Registration details
Analysis ID
439513c375110047c8756bda884127ba
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 management method for medical equipment.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.2700 Pressure Regulator
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Aug 17, 2010
Expiry Date
Aug 17, 2025
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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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 439513c375110047c8756bda884127ba 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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