A non-bioabsorbable, metal device intended to be implanted in a non-neurovascular blood vessel, permanently or long-term, to occlude blood flow typically for treatment of an aneurysm, tumour (e.g., nephroma, hepatoma, uterine fibroids), and/or arteriovenous ma
| Company | Devices | Share |
|---|---|---|
| Aga Medical Corporation | 19 | 28% |
| Nuvascular, Inc. | 14 | 21% |
| Artio Medical, Inc | 7 | 10% |
| Okami Medical, Inc. | 6 | 9% |
| Artventive Medical Group, Inc. | 5 | 7% |
| Ka Medical Llc | 4 | 6% |
| St. Jude Medical, Inc. | 4 | 6% |
| Merit Medical Systems, Inc. | 3 | 4% |
| Microvention, Inc. | 3 | 4% |
| Embolic Acceleration, Llc | 2 | 3% |
Company = labeler of record on GUDID. 10 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 |
|---|---|---|
| KRD | Device, Vascular, For Promoting Embolization | 40 |
| KRD | Device, Vascular, for Promoting Embolization | 32 |
Use these as the dimensions to specify in a tender line.
67 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Non-neurovascular embolization plug, metallic", from 10 companies. The largest labeler is Aga Medical Corporation with 28% of records.
KRD (Device, Vascular, For Promoting Embolization), KRD (Device, Vascular, for Promoting Embolization)
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.