| Primary Device ID | 20075020052074 |
| NIH Device Record Key | e5f91f95-f817-4a55-b28a-b74a9b937deb |
| Commercial Distribution Discontinuation | 2017-12-01 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Electrodes |
| Version Model Number | PR3827 |
| Company DUNS | 491996556 |
| Company Name | Philips Consumer Lifestyle B.V. |
| 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 | 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00075020052988 [Primary] |
| GS1 | 20075020052074 [Package] Contains: 00075020052988 Package: [10 Units] Discontinued: 2017-12-01 Not in Commercial Distribution |
| NGX | STIMULATOR, MUSCLE, POWERED, FOR MUSCLE CONDITIONING |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-18 |
| Device Publish Date | 2016-08-24 |
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