"Dillon" Nanogert Detection System (Unsterilized)
Taiwan·Risk Class 1·DILON TECHNOLOGIES, INC.·Registered Jul 31, 2015 – Jul 31, 2025Cancelled- Analysis ID
- a949442302577dbf26b95094c0d730a5
- Customs Code
- DHA09401553504
- Manufacturer
- DILON TECHNOLOGIES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BESTCHAIN HEALTHTAIWAN CO., LTD.
- Intended Use
- Limited to the first level identification range of nuclear medical ingestion probe (P.1320) under the management measures for medical equipment.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1320 核醫攝取探頭
- Import Information
- QMS/QSD;; 輸入
- Registration Date
- Jul 31, 2015
- Expiry Date
- Jul 31, 2025
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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 a949442302577dbf26b95094c0d730a5 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.