| Primary Device ID | 00817846020303 |
| NIH Device Record Key | e62cdae2-01cd-4ea0-8ee5-31cd07aa8a6a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Getinge |
| Version Model Number | KS2460UCOOOG |
| Company DUNS | 118481233 |
| Company Name | Sonic Systems, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00817846020303 [Primary] |
| FLG | Cleaner, Ultrasonic, Medical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-27 |
| Device Publish Date | 2023-07-19 |
| 00817846020303 | KS2460UCOOOG |
| 00817846020297 | KS2460UCOOOD |
| 00817846020280 | KS2460UCOOOA |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() GETINGE 87358238 5877026 Live/Registered |
Getinge AB 2017-03-03 |
![]() GETINGE 87358210 5877025 Live/Registered |
Getinge AB 2017-03-03 |
![]() GETINGE 77062292 not registered Dead/Abandoned |
Getinge Industrier AB 2006-12-12 |
![]() GETINGE 74512630 1942108 Dead/Cancelled |
GETINGE INDUSTRIER AB 1994-04-14 |
![]() GETINGE 73506524 1384149 Dead/Cancelled |
GETINGE INTERNATIONAL INC. 1984-10-31 |