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 |