| Primary Device ID | 08714729421689 |
| NIH Device Record Key | fbf5b8cf-80f8-4565-8ed2-b0e37f7e169c |
| Commercial Distribution Discontinuation | 2019-03-31 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Percuflex™ Plus |
| Version Model Number | M006175284120 |
| 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 Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08714729421689 [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 | 2022-04-25 |
| Device Publish Date | 2015-09-24 |
| 08714729461388 | Ureteral Stent Set |
| 08714729461319 | Ureteral Stent Set |
| 08714729461241 | Ureteral Stent Set |
| 08714729461234 | Ureteral Stent Set |
| 08714729421689 | Ureteral Stent Set |
| 08714729421665 | Ureteral Stent Set |
| 08714729421528 | Ureteral Stent Set |
| 08714729340010 | Ureteral Stent Set |
| 08714729302056 | Ureteral Stent Set |
| 08714729302049 | Ureteral Stent Set |
| 08714729461890 | Ureteral Stent Set |
| 08714729461456 | Ureteral Stent Set |
| 08714729461173 | Ureteral Stent Set |
| 08714729461029 | Ureteral Stent Set |
| 08714729460954 | Ureteral Stent Set |
| 08714729460886 | Ureteral Stent Set |
| 08714729460879 | Ureteral Stent Set |
| 08714729460671 | Ureteral Stent Set |
| 08714729460596 | Ureteral Stent Set |
| 08714729460565 | Ureteral Stent Set |
| 08714729460480 | Ureteral Stent Set |
| 08714729460442 | Ureteral Stent Set |
| 08714729460350 | Ureteral Stent Set |
| 08714729460220 | Ureteral Stent Set |
| 08714729421603 | Ureteral Stent Set |
| 08714729421566 | Ureteral Stent Set |
| 08714729421542 | Ureteral Stent Set |
| 08714729421481 | Ureteral Stent Set |
| 08714729340027 | Ureteral Stent Set |
| 08714729297222 | Ureteral Stent Set |
| 08714729461371 | Ureteral Stent Set |
| 08714729461166 | Ureteral Stent Set |
| 08714729461104 | Ureteral Stent Set |
| 08714729461098 | Ureteral Stent Set |
| 08714729460749 | Ureteral Stent Set |
| 08714729460664 | Ureteral Stent Set |
| 08714729460558 | Ureteral Stent Set |
| 08714729837886 | Ureteral Stent Set |
| 08714729461821 | Ureteral Stent Set |
| 08714729461753 | Ureteral Stent Set |
| 08714729461685 | Ureteral Stent Set |
| 08714729461609 | Ureteral Stent Set |
| 08714729461302 | Ureteral Stent Set |
| 08714729460947 | Ureteral Stent Set |
| 08714729460817 | Ureteral Stent Set |
| 08714729460800 | Ureteral Stent Set |
| 08714729460732 | Ureteral Stent Set |
| 08714729460527 | Ureteral Stent Set |
| 08714729460510 | Ureteral Stent Set |
| 08714729460473 | Ureteral Stent Set |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PERCUFLEX 73374208 1283228 Live/Registered |
Medi-Tech, Incorporated 1982-07-12 |