| Primary Device ID | 00684995530157 | 
| NIH Device Record Key | f21621a0-bf91-4b82-bb23-bb738403c68a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Silicone Tubing, Translucent | 
| Version Model Number | GS75160-19 | 
| 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 | 00684995530157 [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 |