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Regal & Reishang Automatic Analyzer (Unsterilized) - Taiwan Registration d7fb044b9c16e7f2e636d0133b79729a

Access comprehensive regulatory information for Regal & Reishang Automatic Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7fb044b9c16e7f2e636d0133b79729a and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIASORIN DEUTSCHLAND GMBH, 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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d7fb044b9c16e7f2e636d0133b79729a
Registration Details
Taiwan FDA Registration: d7fb044b9c16e7f2e636d0133b79729a
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Device Details

Regal & Reishang Automatic Analyzer (Unsterilized)
TW: ็ฆฎ้›…ๅฐš ๅ…จ่‡ชๅ‹•ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d7fb044b9c16e7f2e636d0133b79729a

DHA09401753402

Company Information

Germany

Product Details

Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2160 Individual Photometric Chemistry Analyzer for Clinical Use

Input;; QMS/QSD

Dates and Status

Mar 01, 2017

Mar 01, 2022

Sep 30, 2021

Cancellation Information

Logged out

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