| Primary Device ID | 23700911900635 |
| NIH Device Record Key | 0fd52cec-eaa3-4436-95ac-052bcd7954ca |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Perfusion Clamp |
| Version Model Number | PC1025 |
| Company DUNS | 393146183 |
| Company Name | INSTITUT GEORGES LOPEZ |
| 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 | 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 13700911900638 [Primary] |
| GS1 | 23700911900635 [Package] Contains: 13700911900638 Package: Carton box [6 Units] In Commercial Distribution |
| FKK | Clamp, Line |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-13 |
| Device Publish Date | 2023-06-05 |
| 23700911900642 | The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, di |
| 23700911900635 | The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, di |
| 23700911900628 | The Perfusion Clamp is used for explanted organ recovered with aortic patch. It is a sterile, di |