| Primary Device ID | 00851725007078 |
| NIH Device Record Key | 01bede13-ce5b-4d3c-8e1e-9b95083419b2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NetKonnect |
| Version Model Number | BS-983P |
| Catalog Number | BS-983P |
| Company DUNS | 080352293 |
| Company Name | NKUS LAB |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(949)474-9207 |
| info@nklab.com |
| Storage Environment Humidity | Between 5 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 5 Percent (%) Relative Humidity and 80 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851725007078 [Primary] |
| MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-03-23 |
| Device Publish Date | 2016-10-03 |
| 00851725007108 | NetKonnect - LT |
| 00851725007085 | NetKonnect Option BS-984P (RNS Option) |
| 00851725007078 | NetKonnect Option BS-983P (ReportKonnect Option) |
| 00851725007061 | NetKonnect Option BS-982P (1000 Accounts) |
| 00851725007054 | NetKonnect Option BS-981P (15 Accounts) |
| 00851725007047 | NetKonnect |