A sterile, manually-operated device consisting of a barrel (cylinder) with plunger intended to be used for the administration of a contrast medium into the heart, great vessels, and coronary arteries to study the heart and vessels under x-ray photography. It m
| Company | Devices | Share |
|---|---|---|
| Bayer Medical Care Inc. | 146 | 27% |
| Navilyst Medical, Inc. | 74 | 14% |
| Deroyal Industries, Inc. | 57 | 11% |
| Merit Medical Systems, Inc. | 42 | 8% |
| Coeur, Inc. | 38 | 7% |
| Medical Imaging Solutions International Company | 37 | 7% |
| Medline Industries, Inc. | 35 | 7% |
| Shenzhen Antmed Co., Ltd | 19 | 4% |
| Canadian Hospital Specialties Limited | 19 | 4% |
| Shenzhen Boon Medical Supply Co., Ltd. | 18 | 3% |
| Union Medical Shenzhen Co.,Ltd. | 17 | 3% |
| Argon Critical Care Systems Singapore Pte. Ltd. | 9 | 2% |
Company = labeler of record on GUDID. 19 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 |
|---|---|---|
| DXT | Injector And Syringe, Angiographic | 340 |
| DXT | Injector and syringe, angiographic | 93 |
| DXT | INJECTOR AND SYRINGE, ANGIOGRAPHIC | 55 |
| FMF | Syringe, piston | 53 |
| LNH | System, Nuclear Magnetic Resonance Imaging | 13 |
| IZI | System, x-ray, angiographic | 12 |
Use these as the dimensions to specify in a tender line.
533 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Angiographic syringe", from 19 companies. The largest labeler is Bayer Medical Care Inc. with 27% of records.
DXT (Injector And Syringe, Angiographic), DXT (Injector and syringe, angiographic), DXT (INJECTOR AND SYRINGE, ANGIOGRAPHIC), FMF (Syringe, piston)
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.