| Primary Device ID | H6711002021 |
| NIH Device Record Key | 4820e776-8072-4771-be31-0cddb0b5901d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DELTA-FLOW |
| Version Model Number | T-Configuration |
| Catalog Number | 100-202 |
| Company DUNS | 094651270 |
| Company Name | UTAH MEDICAL PRODUCTS, 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 | false |
| 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 | 800-533-4984 |
| customer@utahmed.com |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | H6711002020 [Primary] |
| HIBCC | H6711002021 [Package] Contains: H6711002020 Package: Box [50 Units] In Commercial Distribution |
| KRA | Catheter, Continuous Flush |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-18 |
| Device Publish Date | 2016-09-23 |
| H6711002051 | CONTINUOUS FLUSH DEVICE, 3CC/HR FLOW RATE, Y-CONFIGURATION, BLUE W/TAB |
| H6711002041 | CONTINUOUS FLUSH DEVICE, 3CC/HR FLOW RATE, MALE, BLUE, W/TAB |
| H6711002021 | CONTINUOUS FLUSH DEVICE, T-CONFIGURATION, 3CC/HR FLOW RATE |