| Primary Device ID | 20884838007806 |
| NIH Device Record Key | cd6a3e4c-f682-4fc6-b8f1-f54bf82f4b58 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 989803149901 |
| Catalog Number | 989803149901 |
| Company DUNS | 078628040 |
| Company Name | Philips Medical Systems |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| Phone | +1(999)999-9999 |
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| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20884838007806 [Primary] |
| DRX | Electrode, electrocardiograph |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2017-05-17 |