Taiwan FDA registration aa46ee7b992efe57ee9ade46d448627b

"Arnold" ankang bone tissue sectioning system

TW: “亞諾”安康骨組織切片系統
Taiwan flagTaiwan·Risk Class 2·Vascular Solutions LLC;; Viant San Antonio, Inc.·Registered Jan 11, 2019 – Jan 11, 2029Active
Registration details
Analysis ID
aa46ee7b992efe57ee9ade46d448627b
Customs Code
DHA05603194100
Company information
Manufacturer Country
United States
Authorized Representative
TELEFLEX MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1075 腸胃科-泌尿科生檢器械
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Jan 11, 2019
Expiry Date
Jan 11, 2029
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About this record

Access comprehensive regulatory information for "Arnold" ankang bone tissue sectioning system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aa46ee7b992efe57ee9ade46d448627b and manufactured by Vascular Solutions LLC;; Viant San Antonio, Inc.. The authorized representative in Taiwan is TELEFLEX MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Spartronics Watertown, LLC;; Vascular Solutions LLC, 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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