| Primary Device ID | 00653405987614 |
| NIH Device Record Key | 769af079-3789-4976-85f4-fe9793bb2f9d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MacroLyte |
| Version Model Number | 400-2100 |
| Catalog Number | 6050P |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 50 |
| 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 | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00653405987614 [Unit of Use] |
| GS1 | 20653405987618 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-16 |
| Device Publish Date | 2021-08-06 |
| 20653405007330 | MACROLYTE INFANT DISPERSIVE ELECTRODE |
| 20653405007293 | MACROLYTE PREMIE DISPERSIVE ELECTRODE |
| 20653405007262 | MACROLYTE PEDIATRIC DUAL DISPERSIVE ELECTRODE |
| 20653405007224 | MACROLYTE PEDIATRIC DISPERSIVE ELECTRODE |
| 20653405007187 | MACROLYTE PEDIATRIC DUAL DISPERSIVE ELECTRODE |
| 20653405007019 | MACROLYTE DISPERSIVE ELECTRODE |
| 20653405006999 | MACROLYTE DISPERSIVE ELECTRODE |
| 00653405987614 | GROUND PAD:AD;SGN FOIL, COOPER |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MACROLYTE 73562513 1390441 Live/Registered |
CONSOLIDATED MEDICAL EQUIPMENT, INC. 1985-10-10 |