Taiwan FDA registration 3eebd8a8c5bc9d1567f75b434f71306b

"Tongda" pressure regulator (unsterilized)

TW: "仟達" 壓力調節器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·The second factory of Zhongli Technology Co., Ltd·Registered Jan 09, 2017 – Jan 09, 2022Cancelled
Registration details
Analysis ID
3eebd8a8c5bc9d1567f75b434f71306b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
RESPTECH 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;; 委託製造
Dates and status
Registration Date
Jan 09, 2017
Expiry Date
Jan 09, 2022
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 "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 3eebd8a8c5bc9d1567f75b434f71306b and manufactured by The second factory of Zhongli Technology 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 Zhongli Technology Co., Ltd. Factory 2;; Tongda Instrument 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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