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Kabon Automated Sample Preparation System (Unsterilized) - Taiwan Registration 3e1025bec2316076005b05453623f1c9

Access comprehensive regulatory information for Kabon Automated Sample Preparation System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e1025bec2316076005b05453623f1c9 and manufactured by COPAN WASP S.R.L.. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details. 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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3e1025bec2316076005b05453623f1c9
Registration Details
Taiwan FDA Registration: 3e1025bec2316076005b05453623f1c9
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Device Details

Kabon Automated Sample Preparation System (Unsterilized)
TW: ๅก้‚ฆๅ…จ่‡ชๅ‹•ๆจฃๅ“่ฃฝๅ‚™็ณป็ตฑ(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

3e1025bec2316076005b05453623f1c9

DHA09402256402

Company Information

Italy

Product Details

Limited to the classification and grading management of medical devices, "turbidimetric meter for clinical use (A.2700)" and "microtitration dilution and dispensing device (C.2500)" level 1 identification range.

A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology

A.2700 ่‡จๅบŠไฝฟ็”จ็š„ๆฏ”ๆฟ่จˆ;; C.2500 ๅพฎๆปดๅฎš็จ€้‡‹ๅŠๅˆ†้…ๅ™จๆ

Input;; QMS/QSD

Dates and Status

May 20, 2021

May 20, 2026