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Edwards osmotic analyzer (unsterilized) - Taiwan Registration c983787f429879af7bad1227d6ff826e

Access comprehensive regulatory information for Edwards osmotic 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 c983787f429879af7bad1227d6ff826e and manufactured by ADVANCED INSTRUMENTS, LLC. The authorized representative in Taiwan is BIOWAY CORPORATION.

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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c983787f429879af7bad1227d6ff826e
Registration Details
Taiwan FDA Registration: c983787f429879af7bad1227d6ff826e
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Device Details

Edwards osmotic analyzer (unsterilized)
TW: โ€œ่‰พๅพ—็ด›ๆ€โ€ๆปฒ้€ๅฃ“ๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1

Registration Details

c983787f429879af7bad1227d6ff826e

DHA04400614905

Company Information

United States

Product Details

It is limited to the first level identification scope of the permeameter (A.2730) for clinical use.

A Clinical chemistry and clinical toxicology

A.2730 Permeameter for clinical use

import

Dates and Status

Sep 12, 2007

Sep 12, 2027