"Dillon" Nanogert Detection System (Unsterilized)
Taiwan·Risk Class 1·DILON TECHNOLOGIES, INC.·Registered Oct 01, 2021 – Oct 31, 2025Expired- Analysis ID
- 1b4df1e6a52f5f0f5a28d82c806fb376
- Customs Code
- DHA08401553508
- Manufacturer
- DILON TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BESTCHAIN HEALTHTAIWAN CO., LTD.
- 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 measures for medical devices.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1320 核醫攝取探頭
- Import Information
- Input;; QMS/QSD
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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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.