A device typically considered to be a component of an x-ray film cassette used in diagnostic x-ray applications. It is typically used in pairs with double side emulsion x-ray film. It consists of a backing material, e.g., cardboard, plastic or metal; a reflect
| Company | Devices | Share |
|---|---|---|
| Carestream Health, Inc. | 105 | 81% |
| Flow X Ray Corporation | 24 | 19% |
Company = labeler of record on GUDID. 2 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| EAM | Screen, intensifying, radiographic | 113 |
| IXA | Cassette, radiographic film | 31 |
| EAM | Screen, Intensifying, Radiographic | 24 |
Use these as the dimensions to specify in a tender line.
129 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "X-ray intensifying screen", from 2 companies. The largest labeler is Carestream Health, Inc. with 81% of records.
EAM (Screen, intensifying, radiographic), IXA (Cassette, radiographic film), EAM (Screen, Intensifying, Radiographic)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.