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Fujifilm Assay Starch/Dry Test Piece - Taiwan Registration 847a4b20e2c147dadbe1a21fbb7f8e9f

Access comprehensive regulatory information for Fujifilm Assay Starch/Dry Test Piece in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 847a4b20e2c147dadbe1a21fbb7f8e9f and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Nakanuma Office. The authorized representative in Taiwan is HUNG CHONG CORP..

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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847a4b20e2c147dadbe1a21fbb7f8e9f
Registration Details
Taiwan FDA Registration: 847a4b20e2c147dadbe1a21fbb7f8e9f
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Device Details

Fujifilm Assay Starch/Dry Test Piece
TW: ๅฏŒๅฃซๆธฌๅฎšๆพฑ็ฒ‰/ไนพๅผ่ฉฆ็‰‡
Risk Class 2

Registration Details

847a4b20e2c147dadbe1a21fbb7f8e9f

DHA00601605903

Product Details

Measure the concentration of starch in serum and plasma.

A Clinical chemistry and clinical toxicology

A.1070 ๆพฑ็ฒ‰้…ถ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Feb 27, 2006

Feb 27, 2026