"Acerys" double-tube syringe
- Analysis ID
- 7e032865509190183fe86f151c440b8c
- Customs Code
- DHA00602339905
- Manufacturer
- ARTHREX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Sinjet Limited
- 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
- Registration Date
- Apr 06, 2012
- Expiry Date
- Apr 06, 2017
- Cancellation Date
- Nov 26, 2019
- Status
- Logged out
- Reason
- 未展延而逾期者
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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.