Next Generation NetKonnect
Next Generation NetKonnect is Windows software that displays patient monitoring information from a Nihon Kohden monitoring network on client computers. It provides remote access to vital…
Next Generation NetKonnect is Windows software that displays patient monitoring information from a Nihon Kohden monitoring network on client computers. It provides remote access to vital signs, waveforms and alarm-event information alongside the primary monitoring system.
The software receives data through a network gateway and establishes communication with connected Nihon Kohden devices. It can show information for one patient or multiple patients in near real time.
Listed Item
NGNK audio, touch, unicast, data storage
History and Display
Available history views include graphical or tabular trends, noninvasive blood pressure records, hemodynamic lists, arrhythmia and ST recall, full-disclosure ECG and 12-lead analysis. These displays use information generated by the bedside or central monitors. NetKonnect does not itself detect arrhythmias or determine new alarm conditions.
Who Else Makes It
Concentrated in Guangdong (6), Jiangsu (1), Hebei (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Amphenol Medical Technologies (Dongguan) Co., Ltd. | Dongguan | Guangdong | Contract manufacturer | 77 |
| Shenzhen Mindray BIO-Medical Electronics Co., Ltd. | Shenzhen | Guangdong | Specification developer | 61 |
| GE Medical Systems (China) Co., Ltd. | Wuxi | Jiangsu | Contract manufacturer | 57 |
| Edan Instruments, Inc. | Shenzhen | Guangdong | Contract manufacturer | 56 |
| Shenzhen Comen Medical Instruments Co., Ltd. | Shenzhen | Guangdong | Contract manufacturer | 24 |
| Contec Medical Systems Co., Ltd. | Qinhuangdao | Hebei | Manufacturer | 22 |
| Guangdong Biolight Meditech Co., Ltd. | Zhuhai | Guangdong | Manufacturer | 19 |
| Shanghai Draeger Medical Instrument Co., Ltd. | Shanghai | Shanghai | Contract manufacturer | 4 |
| General Meditech, Inc. | Shenzhen | Guangdong | Complaint-file establishment | 3 |
Record
| Listed by | Nihon Kohden Digital Health Solutions, LLC., United States |
|---|---|
| FDA product code | MHX |
| Device type | Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) |
| Device class | Class 2 |
| Regulation | 21 CFR 870.1025 |
| Establishment | Manufacturer |
| 510(k) | K220989 |
| Record published | 2022-08-31 |
| Record revised | 2025-01-29 (version 3) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Prescription | Prescription only |
| Label carries | serial number |
| Storage | Storage environment temperature -40 to 65 °C; Special storage condition: non-condensing; Storage environment humidity 5 to 95 % RH |
| Distribution end date | 2023-10-20 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| NGNK-6803-T | In distribution | |
| NGNK-6804-T | In distribution | |
| NGNK-6803-M | In distribution | |
| NGNK-6804 | In distribution | |
| NGNK-6804-M | In distribution | |
| NGNK-6803 | In distribution | |
| NGNK-6801 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Fukuda Denshi | Fukuda Denshi Co., Ltd. | 326 |
| Welch Allyn, Inc. | Welch Allyn, Inc. | 266 |
| Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | Nihon Kohden Corp. | 205 |
| Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms) | Nihon Kohden America, Inc. | 139 |
| Surveyor Central | Mortara Instrument, Inc. | 71 |
| Tempus Pro | Remote Diagnostic Technologies Ltd. | 44 |
| Surveyor S12 | Mortara Instrument, Inc. | 38 |
| Ultraview | Spacelabs Healthcare (Washington), Inc | 29 |
| Surveyor S19 | Mortara Instrument, Inc. | 26 |
| Vital Signs™ | AirLife Finland Oy | 23 |
| Patient Monitor | Edan Instruments, Inc. | 22 |
| Telemetry Accessories | Philips Medizin Systeme Böblingen GmbH | 21 |
Showing 12 of 589. All products under Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K220989 | 2022-07-29 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.