| Primary Device ID | 08714729459286 |
| NIH Device Record Key | 17517f61-a177-4bd1-a0b0-a95430163ccc |
| Commercial Distribution Discontinuation | 2023-10-08 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Percuflex™ |
| Version Model Number | M006145383050 |
| 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 | 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 | 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 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 | 08714729459286 [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 | 2024-04-03 |
| Device Publish Date | 2015-09-24 |
| 08714729788423 | Ureteral Stent Set |
| 08714729788362 | Ureteral Stent Set |
| 08714729788324 | Ureteral Stent Set |
| 08714729788300 | Ureteral Stent Set |
| 08714729788294 | Ureteral Stent Set |
| 08714729788287 | Ureteral Stent Set |
| 08714729788270 | Ureteral Stent Set |
| 08714729788263 | Ureteral Stent Set |
| 08714729788256 | Ureteral Stent Set |
| 08714729788249 | Ureteral Stent Set |
| 08714729788225 | Ureteral Stent Set |
| 08714729788218 | Ureteral Stent Set |
| 08714729788201 | Ureteral Stent Set |
| 08714729788195 | Ureteral Stent Set |
| 08714729788188 | Ureteral Stent Set |
| 08714729788164 | Ureteral Stent Set |
| 08714729788157 | Ureteral Stent Set |
| 08714729788140 | Ureteral Stent Set |
| 08714729788126 | Ureteral Stent Set |
| 08714729788102 | Ureteral Stent Set |
| 08714729788096 | Ureteral Stent Set |
| 08714729788089 | Ureteral Stent Set |
| 08714729788072 | Ureteral Stent Set |
| 08714729788041 | Ureteral Stent Set |
| 08714729785361 | Ureteral Stent Set |
| 08714729779384 | Ureteral Stent Set |
| 08714729775966 | Ureteral Stent Set |
| 08714729458838 | Ureteral Stent Set |
| 08714729788232 | Ureteral Stent Set |
| 08714729778400 | Ureteral Stent Set |
| 08714729775881 | Ureteral Stent Set |
| 08714729775843 | Ureteral Stent Set |
| 08714729775829 | Ureteral Stent Set |
| 08714729775775 | Ureteral Stent Set |
| 08714729458470 | Ureteral Stent Set |
| 08714729458197 | Ureteral Stent Set |
| 08714729419396 | Ureteral Stent |
| 08714729788355 | Ureteral Stent Set |
| 08714729788171 | Ureteral Stent Set |
| 08714729788133 | Ureteral Stent Set |
| 08714729788058 | Ureteral Stent Set |
| 08714729777809 | Ureteral Stent Set |
| 08714729775959 | Ureteral Stent Set |
| 08714729775874 | Ureteral Stent Set |
| 08714729775850 | Ureteral Stent Set |
| 08714729775812 | Ureteral Stent Set |
| 08714729459286 | Ureteral Stent Set |
| 08714729458654 | Ureteral Stent Set |
| 08714729458562 | Ureteral Stent Set |
| 08714729788331 | Ureteral Stent Set |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERCUFLEX 73374208 1283228 Live/Registered |
Medi-Tech, Incorporated 1982-07-12 |