Taiwan FDA registration 7e032865509190183fe86f151c440b8c

"Acerys" double-tube syringe

TW: “艾思瑞斯”雙管注射器
Taiwan flagTaiwan·Risk Class 2·ARTHREX, INC.·Registered Apr 06, 2012 – Apr 06, 2017Cancelled
Registration details
Analysis ID
7e032865509190183fe86f151c440b8c
Customs Code
DHA00602339905
Company information
Manufacturer
ARTHREX, INC.
Manufacturer Country
United States
Authorized Representative
Sinjet Limited
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J.5860 活塞式注射筒
Import Information
import
Dates and status
Registration Date
Apr 06, 2012
Expiry Date
Apr 06, 2017
Cancellation Date
Nov 26, 2019
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Acerys" double-tube syringe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7e032865509190183fe86f151c440b8c and manufactured by ARTHREX, INC.. The authorized representative in Taiwan is Sinjet Limited.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TRANSCOJECT GMBH;; Arthrex, Inc., 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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