A material which is used to establish known points of reference for an assay intended to be used for the qualitative and/or quantitative detection of immunoglobulin A (IgA) antibodies to Adenovirus in a clinical specimen.
| Company | Devices | Share |
|---|---|---|
| Microvention, Inc. | 63 | 100% |
Company = labeler of record on GUDID. 1 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 | 36 |
| HCG | DEVICE, NEUROVASCULAR EMBOLIZATION | 27 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
63 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Adenovirus immunoglobulin A (IgA) antibody IVD, calibrator", from 1 companies. The largest labeler is Microvention, Inc. with 100% of records.
KRD (Device, Vascular, for Promoting Embolization), HCG (DEVICE, NEUROVASCULAR 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.