| Primary Device ID | 00616784695532 |
| NIH Device Record Key | 7a437728-2370-4a6a-a774-7b2de33fc1e5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Insulin Syringe |
| Version Model Number | 6955 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 10 |
| 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 | 00616784695501 [Unit of Use] |
| GS1 | 00616784695518 [Primary] |
| GS1 | 00616784695525 [Package] Contains: 00616784695518 Package: Box [10 Units] In Commercial Distribution |
| GS1 | 00616784695532 [Package] Contains: 00616784695525 Package: Case [5 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 | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 00616784695938 | 6959 |
| 00616784695839 | 6958 |
| 00616784695730 | 6957 |
| 00616784695631 | 6956 |
| 00616784695532 | 6955 |
| 00616784695433 | 6954 |
| 00616784695334 | 6953 |
| 00616784695235 | 6952 |
| 00616784695136 | 6951 |
| 00616784695037 | 6950 |
| 00616784694931 | 6949 |
| 00616784694832 | 6948 |
| 00616784694733 | 6947 |
| 00616784694634 | 6946 |
| 00616784694535 | 6945 |
| 00616784694436 | 6944 |
| 00616784694337 | 6943 |
| 00616784694238 | 6942 |
| 00616784694139 | 6941 |
| 00616784694030 | 6940 |