| Primary Device ID | 10850017259031 |
| NIH Device Record Key | 548b95bb-067e-47f2-9a23-709346d5a2dd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Luther Needlesafe Products |
| Version Model Number | 22150001 |
| Catalog Number | 22150001 |
| Company DUNS | 117440613 |
| Company Name | Luther Needlesafe Products, LLC |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850017259034 [Primary] |
| GS1 | 10850017259031 [Package] Contains: 00850017259034 Package: Inner Box [50 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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-05-09 |
| Device Publish Date | 2023-05-01 |
| 00850017259058 | Mini-Midline Extended Dwell Peripheral Catheter - 24Ga, 1.25” |
| 10850017259048 | Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.75” |
| 10850017259031 | Mini-Midline Extended Dwell Peripheral Catheter - 22Ga, 1.50” |
| 10850017259024 | Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.75” |
| 10850017259017 | Mini-Midline Extended Dwell Peripheral Catheter - 20Ga, 1.50” |
| 10850017259000 | Mini-Midline Extended Dwell Peripheral Catheter - 18Ga, 1.75” |