Primary Device ID | 40860008600552 |
NIH Device Record Key | e5458c0b-d04d-42aa-9267-ebdc55eb35f1 |
Commercial Distribution Discontinuation | 2019-07-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | CompoSeal Slim |
Version Model Number | 9029701 |
Catalog Number | 9029701 |
Company DUNS | 315654579 |
Company Name | Fresenius Kabi AG |
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 | true |
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 |