Primary Device ID | 08714729460879 |
NIH Device Record Key | 4f7ff9ee-8583-451d-b571-107bac7795cf |
Commercial Distribution Discontinuation | 2021-10-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Percuflex™ Plus |
Version Model Number | M006175263060 |
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 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 | 08714729460879 [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 | 2023-08-28 |
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 |