| Primary Device ID | 16958697600427 |
| NIH Device Record Key | 86f55263-1430-41bf-86c3-671e0195aa25 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SOL-Guard Safety Needle |
| Version Model Number | 22G x 1 1/2" |
| Catalog Number | SND488 |
| Company DUNS | 543007373 |
| Company Name | ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER 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 | false |
| 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 | 06958697600420 [Primary] |
| GS1 | 16958697600427 [Package] Contains: 06958697600420 Package: [100 Units] In Commercial Distribution |
| GS1 | 26958697600424 [Package] Package: [10 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 | 2021-01-18 |
| Device Publish Date | 2021-01-08 |
| 16958697600427 | A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the sk |
| 16958697600007 | A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the sk |