Primary Device ID | 08714729788294 |
NIH Device Record Key | a3c887c5-a37d-462c-bf34-2fc44ca0488e |
Commercial Distribution Discontinuation | 2021-12-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Percuflex™ |
Version Model Number | M006145379190 |
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 | 08714729788294 [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 |
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 |