UDI device identifier
Complete Blood Pressure Monitor +EKG BP7900
UDI device identifier 00073796267902 · Omron Healthcare, Inc.
Key facts
| Primary DI | 00073796267902 |
|---|---|
| Brand name | Complete Blood Pressure Monitor +EKG |
| Version or model | BP7900 |
| Catalog number | BP7900 |
| Company | Omron Healthcare, Inc. |
| DUNS number | 054318779 |
| Product code | DPS |
| GMDN term | Multiple vital physiological parameter monitoring system, home-use |
| Premarket submission | K182579 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 1, 2019 |
| Version date | Jun 12, 2025 |
| Description | Blood Pressure Monitor and single channel EKG device. |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: