| Primary Device ID | 00884838094253 |
| NIH Device Record Key | 9a9c140b-d23b-4fe7-9a6b-f2efaaff6b41 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PHILIPS IntelliVue GuardianSoftware |
| Version Model Number | E |
| Company DUNS | 314101143 |
| Company Name | Philips Medizin Systeme Böblingen GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx | |
| Phone | +1(999)999-9999 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838094253 [Primary] |
| DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-12-30 |
| Device Publish Date | 2019-12-20 |
| 00884838085718 | D |
| 00884838081925 | C |
| 00884838094253 | E |