Primary Device ID | 00616784892528 |
NIH Device Record Key | 453e9203-81bc-41bd-9b53-a9d5c3530900 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SecureSafe Syringe With Safety Needle |
Version Model Number | 8925 |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00616784892511 [Unit of Use] |
GS1 | 00616784892528 [Primary] |
GS1 | 00616784892535 [Package] Package: Case [8 Units] In Commercial Distribution |
FMF | Syringe, Piston |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-04 |
Device Publish Date | 2017-10-14 |
00616784893228 | 8932 |
00616784893129 | 8931 |
00616784893020 | 8930 |
00616784892924 | 8929 |
00616784892825 | 8928 |
00616784892726 | 8927 |
00616784892627 | 8926 |
00616784892528 | 8925 |
00616784892320 | 8923 |
00616784892122 | 8921 |
00616784892023 | 8920 |
00616784891729 | 8917 |
00616784891620 | 8916 |
00616784891521 | 8915 |