Primary Device ID | 30845854081659 |
NIH Device Record Key | 4166bbb8-071a-47b5-9bfd-4c20f290d5df |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PLUMEVAC |
Version Model Number | AEVV220 |
Catalog Number | AEVV220 |
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 | 30845854081659 [Primary] |
FYD | APPARATUS, EXHAUST, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-03 |
Device Publish Date | 2020-07-24 |
30845854081659 | PlumeVac Surgical Smoke Evacuator 100V-120V 50/60 Hz |
30845854061040 | PlumeVac Surgical Smoke Evacuator 100V-120V 50/60 Hz |
30845854082458 | Automatic Activation Device for PlumeVac Smoke Plume Evacuator |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PLUMEVAC 86974254 5293052 Live/Registered |
Zimmer, Inc. 2016-04-13 |