| 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 |