Taiwan FDA registration ba3f147d44a8fe371929a609f8eae29f
Dillon Navegett Detection System (Non-Sterile)
TW: 迪龍 奈微格特探測系統 (未滅菌)
Taiwan·Risk Class 1·Dilon Technologies, Inc.·Registered Oct 24, 2024 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- ba3f147d44a8fe371929a609f8eae29f
- Customs Code
- DHA084A0031305
Company information
- Manufacturer
- Dilon Technologies, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- BESTCHAIN HEALTHTAIWAN CO., LTD.
Product details
- Intended Use
- 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.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1320 核醫攝取探頭
- Import Information
- import
Dates and status
- Registration Date
- Oct 24, 2024
- Expiry Date
- Oct 31, 2025
About this record
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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