FDA device listing
MPR2 logO DATALOGGER,Wide range power adapter MPR1/2
FDA device listing 1587834140 · RECO MEDIZINTECHNIK Wolfgang Rentsch eK
Key facts
| Proprietary names | MPR2 logO DATALOGGER,Wide range power adapter MPR1/2 |
|---|---|
| Owner/operator | RECO MEDIZINTECHNIK Wolfgang Rentsch eK |
| Owner/operator number | 10046868 |
| Product codes | GWM |
| Device names | GWM - Device, Monitoring, Intracranial Pressure |
| Device class | Class II |
| Classification regulations (21 CFR) | 882.1620 |
| Review panels | Neurology |
| Registered establishments | RECO MEDIZINTECHNIK WOLFGANG RENTSCH EK |
| Establishment registrations | 3010948104 |
| FEI numbers | 3010948104 |
| Establishment operations | Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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