| Primary Device ID | 20860002576620 |
| NIH Device Record Key | afab9c72-1afa-45f6-9637-2fb44d3da1a7 |
| Commercial Distribution Discontinuation | 2099-10-10 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Maveric Medical LLC |
| Version Model Number | M6002-R |
| Company DUNS | 117229530 |
| Company Name | MAVERIC MEDICAL LLC |
| 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 | 00860002576626 [Primary] |
| GS1 | 10860002576623 [Package] Contains: 00860002576626 Package: Box [100 Units] Discontinued: 2099-10-10 In Commercial Distribution |
| GS1 | 20860002576620 [Package] Contains: 10860002576623 Package: Case [1000 Units] Discontinued: 2099-10-10 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 | 2019-11-05 |
| Device Publish Date | 2019-10-28 |
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