| Primary Device ID | 58032248371878 |
| NIH Device Record Key | fb604f03-1754-488f-9448-435525bdf400 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WOLF-PAK Self Safe Safety IV Catheter |
| Version Model Number | 3718760 |
| Company DUNS | 444776777 |
| Company Name | DELTA MED SPA |
| 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 |
| Outer Diameter | 0.74 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08032248371873 [Primary] |
| GS1 | 38032248371874 [Package] Contains: 08032248371873 Package: case [50 Units] In Commercial Distribution |
| GS1 | 58032248371878 [Package] Contains: 38032248371874 Package: box [4 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 | 2020-01-28 |
| Device Publish Date | 2020-01-20 |
| 58032248372875 | IV safety catheter |
| 58032248371878 | IV safety catheter |