Primary Device ID | 00616784696430 |
NIH Device Record Key | 5e5158b1-bd86-4962-94d4-c41a032bc101 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hypodermic Needle |
Version Model Number | 6964 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 100 |
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 | 00616784696416 [Unit of Use] |
GS1 | 00616784696423 [Primary] |
GS1 | 00616784696430 [Package] Contains: 00616784696423 Package: [10 Units] In Commercial Distribution |
FMI | Needle, Hypodermic, Single Lumen |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-10-23 |
Device Publish Date | 2016-09-24 |
00616784697635 | 6976 |
00616784697536 | 6975 |
00616784697437 | 6974 |
00616784697338 | 6973 |
00616784697239 | 6972 |
00616784697130 | 6971 |
00616784697031 | 6970 |
00616784696935 | 6969 |
00616784696836 | 6968 |
00616784696737 | 6967 |
00616784696638 | 6966 |
00616784696539 | 6965 |
00616784696430 | 6964 |
00616784696331 | 6963 |
00616784696232 | 6962 |
00616784696133 | 6961 |
00616784696034 | 6960 |