| Primary Device ID | M6898250405020 |
| NIH Device Record Key | 5eba120c-9f2a-461c-8fe1-41e9a9d7d9b3 |
| Commercial Distribution Discontinuation | 2021-10-30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MEDIC ENHANCEMENT RESUPPLY |
| Version Model Number | 02 |
| Catalog Number | 82-504-05 |
| Company DUNS | 809773968 |
| Company Name | COMBAT MEDICAL SYSTEMS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 |
|---|---|
| HIBCC | M6898250405020 [Primary] |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-03-24 |
| Device Publish Date | 2018-06-08 |
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