| Primary Device ID | 04053275000028 |
| NIH Device Record Key | 55882c63-7253-4ebf-b3c5-a97a7e3101e0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GETINGE |
| Version Model Number | 6713 |
| Catalog Number | GSS67N Model 6713 |
| Company DUNS | 315435859 |
| Company Name | MAQUET GmbH |
| 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04053275000028 [Primary] |
| FLE | Sterilizer, Steam |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-03-11 |
| Device Publish Date | 2019-02-06 |
| 04053275000035 | 6717 |
| 04053275000028 | 6713 |
| 04053275000011 | 6710 |
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 |