| Primary Device ID | 00884838088573 |
| NIH Device Record Key | 1e081458-4a72-4a8a-bc3d-ae8f390c6704 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | V9-2 |
| Version Model Number | 989605466201 |
| Company DUNS | 063377717 |
| Company Name | Philips Ultrasound, 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838088573 [Primary] |
| IYN | System, imaging, pulsed doppler, ultrasonic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-04-29 |
| Device Publish Date | 2018-11-17 |
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