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 |