| Primary Device ID | 16949236203490 |
| NIH Device Record Key | d09c223c-3f83-48df-a58f-791b17529db4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | safety hypodermic needles |
| Version Model Number | 18Gx1"(1.2x25mm) |
| 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 | 06949236203493 [Primary] |
| GS1 | 16949236203490 [Package] Contains: 06949236203493 Package: [100 Units] In Commercial Distribution |
| GS1 | 26949236203497 [Package] Package: [20 Units] In Commercial Distribution |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-29 |
| Device Publish Date | 2022-11-21 |
| 06949236204070 | 23G×38mmTW |
| 06949236204049 | 23G×25mmTW |
| 06949236204018 | 25G×25mmRW |
| 16949236203605 | 30Gx1/2"(0.31x13mm) |
| 16949236203599 | 27Gx1/2"(0.4x13mm) |
| 16949236203582 | 25Gx1"(0.5x25mm) |
| 16949236203575 | 25Gx5/8"(0.5x16mm) |
| 16949236203568 | 23Gx1"(0.6x25mm) |
| 16949236203551 | 22Gx1 1/2"(0.7x38mm) |
| 16949236203544 | 22Gx1"(0.7x25mm) |
| 16949236203537 | 21Gx1 1/2"(0.8x38mm) |
| 16949236203520 | 21Gx1"(0.8x25mm) |
| 16949236203513 | 20Gx1"(0.9x25mm) |
| 16949236203506 | 18Gx1 1/2"(1.2x38mm) |
| 16949236203490 | 18Gx1"(1.2x25mm) |