Primary Device ID | 20653405001963 |
NIH Device Record Key | c2434b70-6a50-4274-a424-dd6545f93f81 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HELIXAR |
Version Model Number | 60-8432-001 |
Catalog Number | 60-8432-001 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
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 | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 20653405001963 [Primary] |
GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
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 | 2017-04-03 |
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30653405001960 | HELIXAR CART |
20653405001994 | HELIXAR STACKING ADAPTER FOR SYSTEM 5000 ELECTROSURGICAL UNIT STACKING ADAPTER |
20653405001987 | SMOKE KIT, HELIXAR AER DEFENSE DOOR ASSEMBLY |
20653405001963 | HELIXAR CART |
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10653405001966 | HELIXAR CART |
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