| Primary Device ID | 05099169710023 |
| NIH Device Record Key | cf23014f-9d37-46f5-bb58-7335b6dcef85 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | VitaloJAK |
| Version Model Number | 7100 |
| Company DUNS | 219683489 |
| Company Name | VITALOGRAPH (IRELAND) LIMITED |
| 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 | false |
| OTC Over-The-Counter | false |
| Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Storage Environment Humidity | Between 10 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05099169710023 [Package] Contains: 15099169710020 Package: [1 Units] In Commercial Distribution |
| GS1 | 15099169710020 [Primary] |
| DSH | RECORDER, MAGNETIC TAPE, MEDICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-08 |
| Device Publish Date | 2018-05-14 |
| 05099169715103 | Base VITALOJAK INTERNATIONAL WEST(1) |
| 05099169710238 | Base VITALOJAK - SHORT CABLE(1) |
| 05099169710023 | Base VitaloJAK UK(1) |
| 05099169715110 | Base VITALOJAK |