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Dillon Navegett Detection System (Non-Sterile) - Taiwan Registration ba3f147d44a8fe371929a609f8eae29f

Access comprehensive regulatory information for Dillon Navegett Detection System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ba3f147d44a8fe371929a609f8eae29f and manufactured by Dilon Technologies, Inc.. The authorized representative in Taiwan is BESTCHAIN HEALTHTAIWAN CO., LTD..

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ba3f147d44a8fe371929a609f8eae29f
Registration Details
Taiwan FDA Registration: ba3f147d44a8fe371929a609f8eae29f
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Device Details

Dillon Navegett Detection System (Non-Sterile)
TW: ่ฟช้พ ๅฅˆๅพฎๆ ผ็‰นๆŽขๆธฌ็ณป็ตฑ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ba3f147d44a8fe371929a609f8eae29f

DHA084A0031305

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 of medical equipment.

P Radiology Science

P.1320 ๆ ธ้†ซๆ”ๅ–ๆŽข้ ญ

import

Dates and Status

Oct 24, 2024

Oct 31, 2025