| Primary Device ID | 10801741050043 |
| NIH Device Record Key | 1e180e05-7e8f-4f16-bb68-3aa0be326df3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cardiothoracic Adaptor |
| Version Model Number | 072510 |
| Catalog Number | 072510 |
| Company DUNS | 016898496 |
| Company Name | C. R. Bard, Inc. |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00801741050046 [Primary] |
| GS1 | 10801741050043 [Package] Contains: 00801741050046 Package: CA [10 Units] In Commercial Distribution |
| GCE | ADAPTOR, CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-30 |
| Device Publish Date | 2020-09-22 |
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