| Primary Device ID | 00685447001041 |
| NIH Device Record Key | 2f54b45f-d1f4-45a4-ba37-a7a3af843c54 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PowerWire Radiofrequency GuideWire Kit |
| Version Model Number | EWK35-250-10-6S |
| Company DUNS | 249225954 |
| Company Name | Baylis Médicale Cie 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 | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00685447001041 [Primary] |
| PDU | Catheter For Crossing Total Occlusions |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-13 |
| 00685447002161 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447002154 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447002147 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001089 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001072 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001065 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001058 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001041 | PowerWire RF GuideWire; RFP-100A Connector Cable |
| 00685447001034 | PowerWire RF GuideWire; RFP-100A Connector Cable |