| Primary Device ID | 03700512925026 |
| NIH Device Record Key | e2c57808-cf61-49f5-b32f-82ef6dcfcb1c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Irrigation Tube |
| Version Model Number | OSG00499E10ST35 |
| Catalog Number | Z263001 |
| 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 | 03700512905028 [Primary] |
| GS1 | 03700512915027 [Package] Contains: 03700512905028 Package: Pouch [10 Units] In Commercial Distribution |
| GS1 | 03700512925026 [Package] Contains: 03700512915027 Package: Box [10 Units] In Commercial Distribution |
| GBX | Catheter, Irrigation |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-04-23 |
| Device Publish Date | 2018-04-06 |
| 03700512925040 | OSG01199E5ST35 |
| 03700512925033 | OSG01199ST35 |
| 03700512925026 | OSG00499E10ST35 |
| 03700512925019 | OSG00499E5ST35 |
| 03700512925002 | OSG00499ST35 |
| 03700512915263 | ODG05599E5ST35 |
| 03700512925071 | OSG03499ST35 |
| 03700512925064 | OSG03399E5ST35 |