| Primary Device ID | 20886333201352 |
| NIH Device Record Key | 70e4643b-2bef-444b-bbec-eee31984b991 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arterial Extensions |
| Version Model Number | 041115002A |
| Catalog Number | 041115002A |
| Company DUNS | 140727624 |
| Company Name | ARGON MEDICAL DEVICES, INC. |
| 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 | 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 |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com | |
| Phone | 1.800.927.4669 |
| Customer.Service@argonmedical.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333201358 [Primary] |
| GS1 | 20886333201352 [Package] Contains: 00886333201358 Package: Box [25 Units] In Commercial Distribution |
| DTL | Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-09 |
| 20886333201352 | Arterial Extensions 6" PVC Extension Tube w/Male Luer Lock and Stopcock |
| 20886333201321 | Arterial Extensions 7Ft. PVC Extension w/Stopcock and Male Luer Lock Adaptor |