| Primary Device ID | 20685447001021 |
| NIH Device Record Key | d4f171c6-dfc2-4f77-83a2-d2490960ffd9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Adult Dispersive Electrode |
| Version Model Number | RFA-GP-BAY |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00685447001027 [Primary] |
| GS1 | 10685447001024 [Package] Contains: 00685447001027 Package: [25 Units] In Commercial Distribution |
| GS1 | 20685447001021 [Package] Contains: 10685447001024 Package: [4 Units] In Commercial Distribution |
| JOS | Electrode, Electrosurgical |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-02-03 |
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| 00685447019572 - VersaCross™ Large Access Solution | 2025-03-05 Large Access Solution |