Primary Device ID | 00685447001072 |
NIH Device Record Key | b9fa643c-4af2-4bde-a45c-99edd6645d14 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PowerWire Radiofrequency GuideWire Kit |
Version Model Number | EWK35-250-12-6A-30-05 |
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 | 00685447001072 [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 |