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"Fischer" Spectrophotometer for clinical use (Non-sterile) - Taiwan Registration 893b5d6b70c8205351cb854205d68edd

Access comprehensive regulatory information for "Fischer" Spectrophotometer for clinical use (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 893b5d6b70c8205351cb854205d68edd and manufactured by FISCHER ANALYSEN INSTRUMENTE GMBH. The authorized representative in Taiwan is PRINCETON INTERNATIONAL INDUSTRIES TAIWAN 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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893b5d6b70c8205351cb854205d68edd
Registration Details
Taiwan FDA Registration: 893b5d6b70c8205351cb854205d68edd
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Device Details

"Fischer" Spectrophotometer for clinical use (Non-sterile)
TW: "่ฒ้›ช" ่‡จๅบŠไฝฟ็”จ็š„ๅˆ†ๅ…‰ๅ…‰ๅบฆ่จˆ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

893b5d6b70c8205351cb854205d68edd

Ministry of Health Medical Device Import Registration No. a00008

DHA084a0000800

Company Information

Product Details

A Clinical chemistry and clinical toxicology

A2300 Colorimeter, photometer, or spectrophotometer for clinical use

Dates and Status

Oct 27, 2021

Oct 31, 2022

Cancellation Information

Logged out

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