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"Dillon" Nanogert Detection System (Unsterilized) - Taiwan Registration 1b4df1e6a52f5f0f5a28d82c806fb376

Access comprehensive regulatory information for "Dillon" Nanogert Detection System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1b4df1e6a52f5f0f5a28d82c806fb376 and manufactured by DILON TECHNOLOGIES, INC.. The authorized representative in Taiwan is BESTCHAIN HEALTHTAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DILON TECHNOLOGIES, INC., 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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1b4df1e6a52f5f0f5a28d82c806fb376
Registration Details
Taiwan FDA Registration: 1b4df1e6a52f5f0f5a28d82c806fb376
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Device Details

"Dillon" Nanogert Detection System (Unsterilized)
TW: "่ฟช้พ" ๅฅˆๅพฎๆ ผ็‰นๆŽขๆธฌ็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

1b4df1e6a52f5f0f5a28d82c806fb376

DHA08401553508

Company Information

United States

Product Details

It is limited to the first-level identification scope of the nuclear medicine ingestion probe (P.1320) of the classification and grading management measures for medical devices.

P Radiology Science

P.1320 ๆ ธ้†ซๆ”ๅ–ๆŽข้ ญ

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025

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