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"Schiller" Argus patient monitor - Taiwan Registration 477c0d83c6995c303fc22a9a1a290344

Access comprehensive regulatory information for "Schiller" Argus patient monitor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 477c0d83c6995c303fc22a9a1a290344 and manufactured by SCHILLER AG. The authorized representative in Taiwan is GETZ BROS & CO. (BVI), INC., TAIWAN BRANCH.

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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477c0d83c6995c303fc22a9a1a290344
Registration Details
Taiwan FDA Registration: 477c0d83c6995c303fc22a9a1a290344
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Device Details

"Schiller" Argus patient monitor
TW: โ€œๅธญๅ‹’โ€ไบžๆ ผๆ–ฏ็—…ๆ‚ฃ็›ฃ่ฆ–ๅ™จ
Risk Class 3
Cancelled

Registration Details

477c0d83c6995c303fc22a9a1a290344

DHA00602248700

Company Information

Switzerland

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.5310 ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ็ณป็ตฑ

import

Dates and Status

Jul 22, 2011

Jul 22, 2016

Apr 25, 2018

Cancellation Information

Logged out

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