Primary Device ID | 16958697602308 |
NIH Device Record Key | 60112489-f0d9-48ca-a5f4-f139536a14e0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Safety Needle |
Version Model Number | 23G x 1 1/2'' |
Catalog Number | 9760W451 |
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 | 06958697602301 [Primary] |
GS1 | 16958697602308 [Package] Contains: 06958697602301 Package: [100 Units] In Commercial Distribution |
GS1 | 26958697602305 [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 | 2021-01-25 |
Device Publish Date | 2021-01-15 |
16958697602315 | A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the sk |
16958697602308 | A non-dedicated, sharp bevel-edged, hollow tubular device intended to be inserted beneath the sk |