| Primary Device ID | 03700512978015 |
| NIH Device Record Key | 58479ff0-9956-4f4b-9f4b-27aeeaafa200 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OlyCath Straight 0 Eye 4 French |
| Version Model Number | ROTG4000ST245 |
| Catalog Number | OLCAS04 |
| Company DUNS | 401020409 |
| Company Name | Promepla |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 03700512968016 [Primary] |
| GS1 | 03700512978015 [Package] Contains: 03700512968016 Package: Box 1 [10 Units] In Commercial Distribution |
| GS1 | 03700512988014 [Package] Package: Box 2 [6 Units] In Commercial Distribution |
| EYB | Catheter, Ureteral, Gastro-Urology |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-05-14 |
| Device Publish Date | 2020-05-06 |