| Primary Device ID | 20886333209808 |
| NIH Device Record Key | e73d45f4-65af-4ba1-96b9-7855ddb43263 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | First Midcath™ S/L Midline Catheter |
| Version Model Number | 384357 |
| Catalog Number | 384357 |
| 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 | true |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry and Away from Sunlight |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00886333209804 [Primary] |
| GS1 | 20886333209808 [Package] Contains: 00886333209804 Package: Box [5 Units] In Commercial Distribution |
| FOZ | Catheter,Intravascular,Therapeutic,Short-Term Less Than 30 Days |
| 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 | 2016-09-21 |
| 20886333209815 | First Midcath™ S/L Midline Catheter 18ga (4F) 1.35mm x 20cm |
| 20886333209808 | First Midcath™ S/L Midline Catheter 20ga (3F) 0.95mm x 20cm |