| Primary Device ID | 20886333215601 |
| NIH Device Record Key | 6559d639-93c0-4055-a20a-6c50bfca53ba |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arterial Catheter Mini-Kit |
| Version Model Number | 498111 |
| Catalog Number | 498111 |
| 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 | true |
| 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 | 00886333215607 [Primary] |
| GS1 | 20886333215601 [Package] Contains: 00886333215607 Package: Box [10 Units] In Commercial Distribution |
| GDY | Gauze/Sponge, Internal, X-Ray Detectable |
| 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 |
| 20886333215724 | Arterial Catheter Mini-Kit 20ga x3" |
| 20886333215601 | Arterial Catheter Mini-Kit 18ga x 3" |
| 20886333215588 | Arterial Catheter Mini-Kit 20ga x 3" |
| 20886333215564 | Arterial Catheter Mini-Kit 18ga x 6" |
| 20886333215540 | Arterial Catheter Mini-Kit 20ga x 6" |