Taiwan FDA registration a11640eac9ecee598b7f1e0377332cc8

"Accriva" Tenderfoot Incision Instruments (Non-Sterile)

TW: "艾奎發" 腳跟採血器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·Accriva Diagnostics Inc., dba ITC, dba Accumetrics·Registered Oct 06, 2016 – Oct 06, 2021Expired
Registration details
Analysis ID
a11640eac9ecee598b7f1e0377332cc8
License Form
Ministry of Health Medical Device Import No. 017061
Customs Code
DHA09401706108
Company information
Manufacturer Country
United States
Authorized Representative
BEAM INTERNATIONAL INC.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1)
I General and plastic surgical devices
Product Type (Level 2)
I4800 General Surgery Manual Instrument
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 06, 2016
Expiry Date
Oct 06, 2021
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About this record

Access comprehensive regulatory information for "Accriva" Tenderfoot Incision Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a11640eac9ecee598b7f1e0377332cc8 and manufactured by Accriva Diagnostics Inc., dba ITC, dba Accumetrics. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ACCRIVA DIAGNOSTICS, 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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