| Primary Device ID | 10841522119224 |
| NIH Device Record Key | 791900ed-c31c-4e2d-9852-fcfefd1ebbda |
| Commercial Distribution Discontinuation | 2019-03-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Digital Telemetry Transmitter |
| Version Model Number | 90343 |
| Catalog Number | R-90343 |
| Company DUNS | 145581588 |
| Company Name | SPACELABS HEALTHCARE (WASHINGTON), INC |
| 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 | false |
| Serial Number | true |
| 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 |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 0 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10841522119224 [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 | 2019-05-07 |
| Device Publish Date | 2019-03-06 |
| 10841522119385 | ULTRAVIEW DIG TM REFURB |
| 10841522119224 | ULTRAVIEW DIG TM REFURB |
| 10841522108709 | ULTRAVIEW, SYNTH, MPT, 1400MHZ, REFURBISHED |
| 10841522108693 | ULTRAVIEW, SYNTH, MPT, 1400MHZ, REFURBISHED |
| 10841522108365 | ULTRAVIEW DIG TM NB TX,ECG,608-614M |