| Primary Device ID | 00884838083059 |
| NIH Device Record Key | fd4d3831-5c87-4bde-8cb5-198f434c8fb6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | 40009 PercuNav Coaxial Needle Tracker, 20G x 17 cm |
| Version Model Number | 989605428064 |
| Company DUNS | 063377717 |
| Company Name | Philips Ultrasound, Inc. |
| Device Count | 2 |
| DM Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00884838083059 [Primary] |
| GS1 | 00884838083141 [Unit of Use] |
| LLZ | System, image processing, radiological |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[00884838083059]
Ethylene Oxide
[00884838083059]
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| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-25 |
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