Primary Device ID | 00840117334489 |
NIH Device Record Key | fffe1625-bb36-4550-8f97-56eff38f0cd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pre-Filled Saline Flush Syringe,Sterile,5mL |
Version Model Number | 7058 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
Device Count | 30 |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117334489 [Package] Contains: 00840117334496 Package: Case [16 Units] In Commercial Distribution |
GS1 | 00840117334496 [Primary] |
GS1 | 00840117334502 [Unit of Use] |
GS1 | 08401173344960 [Unit of Use] |
NGT | Saline, Vascular Access Flush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-15 |
Device Publish Date | 2024-03-07 |
00810180840163 - DynaSafety Cotton-Tipped Applicators in Sealed Vial,3" | 2024-11-19 |
00840117341210 - Medicine Cups 1oz | 2024-11-05 |
00840117312906 - Resp-O2 Endotracheal Tube Cuffed, 4.0 mm | 2024-11-01 Sterile-EO |
00840117312920 - Resp-O2 Endotracheal Tube Cuffed, 4.5 mm | 2024-11-01 Sterile-EO |
00840117317475 - Resp-O2 Endotracheal Tube Cuffed, 5.0 mm | 2024-11-01 Sterile-EO |
00840117312968 - Resp-O2 Endotracheal Tube Cuffed, 5.5 mm | 2024-11-01 Sterile-Eo |
00840117312982 - Resp-O2 Endotracheal Tube Cuffed, 6.0 mm | 2024-11-01 Sterile-Eo |
00840117313002 - Resp-O2 Endotracheal Tube Cuffed, 6.5 mm | 2024-11-01 Sterile-Eo |