Primary Device ID | 23700911900642 |
NIH Device Record Key | c7e51c7d-8f92-4873-83fa-6aa612bc0e42 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Perfusion Clamp |
Version Model Number | PC715 |
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 | 13700911900645 [Primary] |
GS1 | 23700911900642 [Package] Contains: 13700911900645 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 |