| Primary Device ID | 00616784700830 |
| NIH Device Record Key | cdb59d19-d2a2-4c34-9ccc-4fbf58c0384d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Syringe w/Needle |
| Version Model Number | 7008 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 100 |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 00616784700816 [Unit of Use] |
| GS1 | 00616784700823 [Primary] |
| GS1 | 00616784700830 [Package] Contains: 00616784700823 Package: [4 Units] In Commercial Distribution |
| FMF | Syringe, Piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-23 |
| Device Publish Date | 2016-09-24 |
| 00616784701639 | 7016 |
| 00616784701530 | 7015 |
| 00616784701431 | 7014 |
| 00616784701332 | 7013 |
| 00616784701233 | 7012 |
| 00616784701134 | 7011 |
| 00616784701035 | 7010 |
| 00616784700939 | 7009 |
| 00616784700830 | 7008 |
| 00616784700731 | 7007 |
| 00616784700632 | 7006 |
| 00616784700533 | 7005 |
| 00616784700434 | 7004 |
| 00616784700335 | 7003 |
| 00616784700236 | 7002 |
| 00616784700137 | 7001 |
| 00616784700038 | 7000 |
| 00616784699936 | 6999 |
| 00616784699837 | 6998 |
| 00616784699738 | 6997 |
| 00616784699639 | 6996 |
| 00616784699530 | 6995 |
| 00616784699431 | 6994 |