Primary Device ID | 30845854053144 |
NIH Device Record Key | dcffa341-a075-430a-806d-ba42cc4d9798 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MINIVAC |
Version Model Number | MGEZLINK01 |
Catalog Number | MGEZLINK01 |
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 | true |
Serial Number | false |
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 | 30845854053144 [Primary] |
FYD | APPARATUS, EXHAUST, SURGICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2021-04-14 |
Device Publish Date | 2020-06-18 |
30845854053144 | Automatic Activation Device for MiniVac Smoke Plume Evacuator |
30845854053106 | MiniVac Smoke Evacuation System 220-240V 50/60 Hz |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MINIVAC 85067668 not registered Dead/Abandoned |
HYDROFERA, LLC 2010-06-21 |
MINIVAC 76104318 2886858 Dead/Cancelled |
SKC Inc. 2000-08-07 |
MINIVAC 74205169 1730880 Live/Registered |
MICROTEK MEDICAL, INC. 1991-09-19 |