| Primary Device ID | 00685447006039 |
| NIH Device Record Key | 5ab48590-8a16-4bbc-a6bb-363d1d4072a5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SupraCross RF Wire |
| Version Model Number | SCW0003 |
| Catalog Number | NA |
| 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 |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com | |
| Phone | 5144889801 |
| info@baylismedical.com |
| 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 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 | 00685447006039 [Primary] |
| DXF | Catheter, Septostomy |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-29 |
| Device Publish Date | 2022-11-21 |
| 00685447000990 | SupraCross RF Wire; Connector Cable |
| 00685447006459 | SupraCross RF Wire; Connector Cable |
| 00685447006442 | SupraCross RF Wire; Connector Cable |
| 00685447006435 | SupraCross RF Wire; Connector Cable |
| 00685447006428 | SupraCross RF Wire; Connector Cable |
| 00685447006046 | SupraCross RF Wire; Connector Cable |
| 00685447006039 | SupraCross RF Wire; Connector Cable |
| 00685447006022 | SupraCross RF Wire; Connector Cable |
| 00685447006015 | SupraCross RF Wire; Connector Cable |