"Agfa" digital X-ray imaging system
Taiwan·Risk Class 2·AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.·Registered Nov 13, 2017 – Nov 13, 2022Cancelled- Analysis ID
- 6336f8a8985a95155ecb1eb458e576c4
- Customs Code
- DHAS5603041702
- Manufacturer
- AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.
- Manufacturer Country
- Belgium;;Germany
- Authorized Representative
- AGFA MATERIALS TAIWAN CO., LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.1680 固定式X光系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
- Registration Date
- Nov 13, 2017
- Expiry Date
- Nov 13, 2022
- Cancellation Date
- Apr 12, 2024
- Status
- Logged out
- Reason
- 許可證已逾有效期
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Access comprehensive regulatory information for "Agfa" digital X-ray imaging system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6336f8a8985a95155ecb1eb458e576c4 and manufactured by AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.. The authorized representative in Taiwan is AGFA MATERIALS TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including AGFA N.V., AGFA HEALTHCARE N. V., and 4 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.