Primary Device ID | 04251303302230 |
NIH Device Record Key | 22e1f470-7593-4340-862c-722a869efd48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Karl Storz |
Version Model Number | TM442 |
Catalog Number | 6GF62008UB21 |
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 | 04251303302230 [Primary] |
KQM | Camera, Surgical And Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-26 |
Device Publish Date | 2024-02-16 |
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 |