“CARESTREAM” Digital Radiography Detector
Taiwan·Risk Class 2·MD·Carestream Health, Inc.·Registered Nov 16, 2016 – Nov 16, 2026Active- Analysis ID
- 2340d9f0b0580d4ff97314a2f5b07529
- License Form
- Ministry of Health Medical Device Import No. 029101
- Customs Code
- DHA05602910103
- Manufacturer
- Carestream Health, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- FAITH BIOMED LTD.
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1650 fluoroscopic X-ray image intensifier
- Import Information
- Imported from abroad
- Registration Date
- Nov 16, 2016
- Expiry Date
- Nov 16, 2026
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Access comprehensive regulatory information for “CARESTREAM” Digital Radiography Detector in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2340d9f0b0580d4ff97314a2f5b07529 and manufactured by Carestream Health, Inc.. The authorized representative in Taiwan is FAITH BIOMED LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Carestream Health, 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.