FDA device listing
LiquoGuard 7,LiquoGuard 7 Drainage Set, Length 2000mm REF. 00003501 2351, 00003501 2371, 00003501 2311, 00003501 2471…
FDA device listing 1460177341 · Geckeler
Key facts
| Proprietary names | LiquoGuard 7,LiquoGuard 7 Drainage Set, Length 2000mm REF. 00003501 2351, 00003501 2371, 00003501 2311, 00003501 2471, 00003501 2411 |
|---|---|
| Owner/operator | Geckeler |
| Owner/operator number | 9080465 |
| Premarket submissions | K150898 |
| Product codes | JXG |
| Device names | JXG - Shunt, Central Nervous System And Components |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.5550 |
| Review panels | Neurology |
| Registered establishments | MOELLER MEDICAL GMBH |
| Establishment registrations | 3006611221 |
| FEI numbers | 3002807634 |
| Establishment operations | 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