| Primary Device ID | 08714729789536 |
| NIH Device Record Key | d09ace64-6ff3-43ff-91c2-ce93518a1ac5 |
| Commercial Distribution Discontinuation | 2023-09-29 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Lingeman Percutaneous Tract Kit |
| Version Model Number | M0064501150 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| 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 | true |
| 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 | true |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729789536 [Primary] |
| OFC | Catheter introducer kit |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2024-10-11 |
| Device Publish Date | 2016-09-24 |
| 08714729877523 - EP XT™ | 2026-03-20 Unidirectional Steerable Diagnostic Catheter |
| 08714729877714 - Dynamic XT™ | 2026-03-20 Unidirectional Steerable Diagnostic Catheter |
| 08714729879947 - EP XT™ | 2026-03-20 Unidirectional Steerable Diagnostic Catheter |
| 08714729181088 - Percuflex™ Biliary | 2026-03-19 Biliary Stent with Introducer Kit |
| 08714729181095 - Percuflex™ Biliary | 2026-03-19 Biliary Stent with Introducer Kit |
| 08714729181101 - Percuflex™ Biliary | 2026-03-19 Biliary Stent with Introducer Kit |
| 08714729181118 - Percuflex™ Biliary | 2026-03-19 Biliary Stent with Introducer Kit |
| 08714729181125 - Percuflex™ Biliary | 2026-03-19 Biliary Stent with Introducer Kit |