| Primary Device ID | 00850925007352 |
| NIH Device Record Key | ac3377fa-6698-4939-b219-939cd859b7f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | E2082CG |
| Version Model Number | E2082CG |
| Catalog Number | E2082CG |
| Company DUNS | 066412472 |
| Company Name | NOVUM MEDICAL PRODUCTS 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 | 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 | false |
| OTC Over-The-Counter | false |
| Phone | +1(800)274-2742 |
| info@novummed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850925007352 [Primary] |
| FMS | BED, PEDIATRIC OPEN HOSPITAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-19 |
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