| Primary Device ID | 40331330420007 |
| NIH Device Record Key | e284c837-f7c4-4d4e-843a-72b45121e9c6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Custodiol |
| Version Model Number | 4 x 2000 ml |
| Company DUNS | 316512953 |
| Company Name | Dr. Franz Köhler Chemie GmbH |
| Device Count | 4 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from light |
| Storage Environment Temperature | Between 35 Degrees Fahrenheit and 59 Degrees Fahrenheit |
| Special Storage Condition, Specify | Between 0 and 0 *Protect from light |
| Storage Environment Temperature | Between 35 Degrees Fahrenheit and 59 Degrees Fahrenheit |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04033133002000 [Unit of Use] |
| GS1 | 40331330420007 [Primary] |
| KDL | Set, Perfusion, Kidney, Disposable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-22 |
| 40331330610002 | 6 x 1000 ml |
| 40331330420007 | 4 x 2000 ml |
| 40331330250000 | 2 x 5000 ml |
| 40331330105003 | 10 x 500 ml |
| 40331330050006 | 5000 ml |
| 40331330020009 | 2000 ml |
| 40331330010000 | 1000 ml |
| 40331330005006 | 500 ml |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CUSTODIOL 75093836 2221916 Live/Registered |
Dr. Franz Kohler Chemie GmbH 1996-04-25 |