| Primary Device ID | 00684995530188 |
| NIH Device Record Key | b8610f8a-7dc2-4eee-8c7f-91abd5ad9e14 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Silicone Tubing, Translucent |
| Version Model Number | GS75160-24 |
| Company DUNS | 080524654 |
| Company Name | BENTEC MEDICAL OPCO, LLC |
| 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 | 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 | 00684995530188 [Primary] |
| 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 | 2023-10-30 |
| Device Publish Date | 2023-10-20 |
| 00684995530201 | 28 Fr. x 100 cm |
| 00684995530195 | 26 Fr. x 100 cm |
| 00684995530188 | 24 Fr. x 100 cm |
| 00684995530171 | 22 Fr. x 100 cm |
| 00684995530164 | 20 Fr. x 100 cm |
| 00684995530157 | 19 Fr. x 100 cm |
| 00684995530140 | 18 Fr. x 100 cm |
| 00684995530133 | 16 Fr. x 100 cm |
| 00684995530126 | 15 Fr. x 100 cm |
| 00684995530119 | 14 Fr. x 100 cm |
| 00684995530102 | 12 Fr. x 100 cm |
| 00684995530089 | 10 Fr. x 100 cm |
| 00684995530072 | 9 Fr. x 100 cm |
| 00684995530065 | 8 Fr. x 100 cm |
| 00684995530058 | 7 Fr. x 100 cm |
| 00684995530041 | 6 Fr. x 100 cm |
| 00684995530034 | 5 Fr. x 100 cm |
| 00684995530027 | 4 Fr. x 100 cm |
| 00684995530010 | 3 Fr. x 100 cm |