| Primary Device ID | 04251303300397 |
| NIH Device Record Key | c91b4cf4-c59c-42b3-b37f-37ae7b09bfa6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Karl Storz |
| Version Model Number | TM440 |
| Catalog Number | 6GF62008CA02 |
| Company DUNS | 312523065 |
| Company Name | EIZO GmbH |
| 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 | false |
| 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 | 04251303300397 [Primary] |
| KQM | Camera, Surgical And Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-09-13 |
| Device Publish Date | 2023-01-05 |
| 04251303300397 | LCD Color Monitor |
| 04251303302230 | LCD Color Monitor |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() KARL STORZ 79056906 3705458 Live/Registered |
KARL STORZ SE & Co. KG 2008-05-09 |
![]() KARL STORZ 77216524 3388360 Live/Registered |
KARL STORZ SE & CO. KG 2007-06-27 |
![]() KARL STORZ 75872005 2670809 Live/Registered |
KARL STORZ SE & CO. KG 1999-12-15 |
![]() KARL STORZ 75872004 2539069 Live/Registered |
KARL STORZ SE & CO. KG 1999-12-15 |
![]() KARL STORZ 73315490 not registered Dead/Abandoned |
KARL STORZ GMBH & CO. 1981-06-19 |
![]() KARL STORZ 73274168 not registered Dead/Abandoned |
KARL STORZ GMBH & CO. 1980-08-14 |