| Primary Device ID | 10841522108365 |
| NIH Device Record Key | 2072cdca-acec-460c-adc4-f07c8c5e7055 |
| Commercial Distribution Discontinuation | 2019-03-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Digital Telemetry Transmitter |
| Version Model Number | 90341 |
| Catalog Number | R-90341-05 |
| 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 | 10841522108365 [Primary] |
| DSI | DETECTOR AND ALARM, ARRHYTHMIA |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2019-05-07 |
| Device Publish Date | 2016-12-20 |
| 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 |