"Agfa" digital X-ray imaging system
Taiwan·Risk Class 2·AGFA-GEVAERT HEALTHCARE GMBH;; AGFA N.V.·Registered Sep 01, 2016 – Sep 01, 2021Cancelled- Analysis ID
- 61e381f983540e248a5f4b66b7ace5d2
- Customs Code
- DHA05602877601
- 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
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
- Registration Date
- Sep 01, 2016
- Expiry Date
- Sep 01, 2021
- Cancellation Date
- Sep 23, 2023
- Status
- Logged out
- Reason
- 自行鍵入
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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 61e381f983540e248a5f4b66b7ace5d2 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.