| Primary Device ID | 08714729902980 |
| NIH Device Record Key | 0426a5ea-644f-4a81-88bc-b5202d2a989c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Percuflex™ Plus SureDrive™ |
| Version Model Number | M0061457440 |
| Company DUNS | 021717889 |
| Company Name | BOSTON SCIENTIFIC CORPORATION |
| 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 | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729902980 [Primary] |
| FAD | STENT, URETERAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2026-01-16 |
| Device Publish Date | 2017-11-03 |
| 08714729903130 | Steerable Ureteral Stent Set |
| 08714729903123 | Steerable Ureteral Stent Set |
| 08714729903116 | Steerable Ureteral Stent Set |
| 08714729903109 | Steerable Ureteral Stent Set |
| 08714729903093 | Steerable Ureteral Stent Set |
| 08714729903086 | Steerable Ureteral Stent Set |
| 08714729903079 | Steerable Ureteral Stent Set |
| 08714729903062 | Steerable Ureteral Stent Set |
| 08714729903055 | Steerable Ureteral Stent Set |
| 08714729903048 | Steerable Ureteral Stent Set |
| 08714729903031 | Steerable Ureteral Stent Set |
| 08714729903024 | Steerable Ureteral Stent Set |
| 08714729903017 | Steerable Ureteral Stent Set |
| 08714729903000 | Steerable Ureteral Stent Set |
| 08714729902997 | Steerable Ureteral Stent Set |
| 08714729902980 | Steerable Ureteral Stent Set |
| 08714729902973 | Steerable Ureteral Stent Set |
| 08714729902966 | Steerable Ureteral Stent Set |
| 08714729902959 | Steerable Ureteral Stent Set |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERCUFLEX 73374208 1283228 Live/Registered |
Medi-Tech, Incorporated 1982-07-12 |