Primary Device ID | 30845854081802 |
NIH Device Record Key | 84601207-6e07-4fc9-982f-29958b81c20f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HarmonyAIR |
Version Model Number | QS0022 |
Catalog Number | QS0022 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 2 |
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 | 00724995150068 [Previous] |
GS1 | 00845854081801 [Unit of Use] |
GS1 | 10845854081808 [Direct Marking] |
GS1 | 20845854081805 [Primary] |
GS1 | 30845854081802 [Package] Contains: 20845854081805 Package: Box [2 Units] In Commercial Distribution |
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 | 2020-09-21 |
Device Publish Date | 2020-09-11 |
30845854081826 | AUTO ACTIVE DEVICE, STERIS |
30845854081819 | HARMONYAIR FLUID TRAP, STERIS |
30845854081802 | STERIS VV FILTER 2 PK |
00845854081818 | HARMONYAIR FLUID TRAP, STERIS |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HARMONYAIR 86440989 5087153 Live/Registered |
STERIS Corporation 2014-10-31 |