UDI device identifier
072 Aspiration System FG 00806
UDI device identifier 00857545008097 · Q'APEL MEDICAL LLC
Key facts
| Primary DI | 00857545008097 |
|---|---|
| Brand name | 072 Aspiration System |
| Version or model | FG 00806 |
| Catalog number | AP6072-132 |
| Company | Q'APEL MEDICAL LLC |
| DUNS number | 020937374 |
| Product code | NRY |
| GMDN term | Thrombectomy suction catheter |
| Premarket submission | K222786 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 11, 2023 |
| Version date | May 19, 2025 |
| Description | As part of the 072 Aspiration System, the 072 Aspiration Catheter with a compatible suction pump is indicated for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral - M1 and M2… |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: