| Primary Device ID | 00616784125411 |
| NIH Device Record Key | 39dd3cab-f2f6-4a08-a7af-0ecca473d9dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DynaLube, Sterile, 4 oz. Tube |
| Version Model Number | 1254 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| 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 | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00616784125411 [Primary] |
| GS1 | 00616784125428 [Package] Package: Box [12 Units] In Commercial Distribution |
| GS1 | 00616784125435 [Package] Contains: 00616784125428 Package: Case [6 Units] In Commercial Distribution |
| KMJ | Lubricant, Patient |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-05-31 |
| Device Publish Date | 2022-05-23 |