FDA device listing
NAMIC Contrast Controller,NAMIC Contrast Management System,NAMIC Squeeze Contrast Controller
FDA device listing 1856109143 · Medline Industries, LP
Key facts
| Proprietary names | NAMIC Contrast Controller,NAMIC Contrast Management System,NAMIC Squeeze Contrast Controller |
|---|---|
| Owner/operator | Medline Industries, LP |
| Owner/operator number | 1417592 |
| Premarket submissions | K903493 |
| Product codes | IZI |
| Device names | IZI - System, X-Ray, Angiographic |
| Device class | Class II |
| Classification regulations (21 CFR) | 892.1600 |
| Review panels | Radiology |
| Registered establishments | Medline Canada, Medline Industries, LP - Mexicali (MXC), MEDLINE INDUSTRIES, LP (Northpoint Services), Medline Industries (NAMIC Division) - Glen Falls, Nuevo Laredo Directo al Cliente, PRODUCTOS MEDLINE S.A. DE C.V. |
| Establishment registrations | 1422634, 3004122598, 3007289408, 3015173212, 3015910259, 3045816907 |
| FEI numbers | 1000514656, 3004122598, 3007289408, 3015173212, 3015910259, 3045816907 |
| Establishment operations | Contract Sterilizer, Foreign Exporter, Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database