| Primary Device ID | 00684995510043 | 
| NIH Device Record Key | 45f0e79c-0fcd-4a0f-b00b-b83fd2951033 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Silicone T-Tube | 
| Version Model Number | SU130-1238 | 
| 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 | 00684995510043 [Primary] | 
| PTT | Biliary Catheter For Irrigation And Contrast Injection, Exempt | 
| 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 | 
| 00684995510104 | 7 Fr. x 12 in L | 
| 00684995510098 | 5 Fr. x 12 in L | 
| 00684995510081 | 3 Fr. x 12 in L | 
| 00684995510074 | 2 Fr. x 12 in L | 
| 00684995510067 | 16 Fr. x 12 in L | 
| 00684995510050 | 14 Fr. x 12 in L | 
| 00684995510043 | 12 Fr. x 12 in L | 
| 00684995510036 | 10 Fr. x 12 in L | 
| 00684995510029 | 8 Fr. x 12 in L | 
| 00684995510012 | 6 Fr. x 12 in L | 
| 00684995510005 | 4 Fr. x 12 in L |