| Primary Device ID | 03700512915263 |
| NIH Device Record Key | d4140449-9e73-40df-9a08-258479e4c185 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Irrigation Tube |
| Version Model Number | ODG05599E5ST35 |
| Catalog Number | Y1500070 |
| Company DUNS | 401020409 |
| Company Name | Promepla |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700512905196 [Primary] |
| GS1 | 03700512915263 [Package] Contains: 03700512905196 Package: [5 Units] In Commercial Distribution |
| GS1 | 03700512925262 [Package] Contains: 03700512905196 Package: [20 Units] In Commercial Distribution |
| GBX | Catheter, Irrigation |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-01 |
| Device Publish Date | 2024-10-24 |
| 03700512925040 | OSG01199E5ST35 |
| 03700512925033 | OSG01199ST35 |
| 03700512925026 | OSG00499E10ST35 |
| 03700512925019 | OSG00499E5ST35 |
| 03700512925002 | OSG00499ST35 |
| 03700512915263 | ODG05599E5ST35 |
| 03700512925071 | OSG03499ST35 |
| 03700512925064 | OSG03399E5ST35 |