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"Eleamp" Medical Sealed Injection Source (Unsterilized) - Taiwan Registration f18f59a1a9dcc60b51846b66d94e28a6

Access comprehensive regulatory information for "Eleamp" Medical Sealed Injection Source (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f18f59a1a9dcc60b51846b66d94e28a6 and manufactured by ECKERT & ZIEGLER ISOTOPE PRODUCTS. The authorized representative in Taiwan is GLOBAL MEDICAL SOLUTIONS TAIWAN, LTD..

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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f18f59a1a9dcc60b51846b66d94e28a6
Registration Details
Taiwan FDA Registration: f18f59a1a9dcc60b51846b66d94e28a6
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Device Details

"Eleamp" Medical Sealed Injection Source (Unsterilized)
TW: "้†ซๅˆฉๅฎ‰ๆ™ฎ" ้†ซ็”จๅฏ†ๅฐๅฐ„ๆบ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f18f59a1a9dcc60b51846b66d94e28a6

DHAS4401307807

Company Information

United States

Product Details

It is limited to the first-level identification scope of the "Nuclear Medical Sealing Correction Source (P.1400)" of the Administrative Measures for the Classification and Grading of Medical Devices.

P Radiology Science

P.1400 ้†ซ็”จๅฏ†ๅฐๆ กๆญฃๅฐ„ๆบ

Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input

Dates and Status

Jun 03, 2013

Jun 03, 2028