| Primary Device ID | 06949236205046 |
| NIH Device Record Key | 875fbb4b-afad-4bde-93a5-c13fdb26d123 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | hypodermic syringes |
| Version Model Number | 1ml 25G×25mmRW |
| Company DUNS | 529239746 |
| Company Name | Berpu Medical Technology Co.,Ltd |
| 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 | 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 | 06949236205039 [Primary] |
| GS1 | 06949236205046 [Package] Contains: 06949236205039 Package: [100 Units] In Commercial Distribution |
| GS1 | 06949236205053 [Package] Package: [12 Units] In Commercial Distribution |
| GS1 | 06949236205121 [Package] Package: [10 Units] In Commercial Distribution |
| FMF | Syringe, Piston |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-09 |
| Device Publish Date | 2020-09-01 |
| 06949236205046 | 1ml 25G×25mmRW |
| 06949236205015 | 1ml 23G×25mmTW |
| 06949236205213 | 3ml 25G×25mm RW |