Primary Device ID | 08714729424260 |
NIH Device Record Key | 93b5505e-8c68-4fde-a47b-22b4ff992bcc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Contour™ |
Version Model Number | M006180232090 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 08714729424260 [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 | 2024-09-11 |
Device Publish Date | 2015-09-24 |
08714729159797 | Embolization Particles |
08714729159780 | Embolization Particles |
08714729159773 | Embolization Particles |
08714729159766 | Embolization Particles |
08714729159759 | Embolization Particles |
08714729159742 | Embolization Particles |
08714729159735 | Embolization Particles |
08714729159728 | Embolization Particles |
08714729159711 | Embolization Particles |
08714729159704 | Embolization Particles |
08714729159698 | Embolization Particles |
08714729159681 | Embolization Particles |
08714729159674 | Embolization Particles |
08714729159667 | Embolization Particles |
08714729789505 | Ureteral Stent Set |
08714729789499 | Ureteral Stent Set |
08714729789482 | Ureteral Stent Set |
08714729789475 | Ureteral Stent Set |
08714729789468 | Ureteral Stent Set |
08714729789444 | Ureteral Stent Set |
08714729789437 | Ureteral Stent Set |
08714729789420 | Ureteral Stent Set |
08714729789413 | Ureteral Stent Set |
08714729789406 | Ureteral Stent Set |
08714729789390 | Ureteral Stent Set |
08714729789383 | Ureteral Stent Set |
08714729789376 | Ureteral Stent Set |
08714729789369 | Ureteral Stent Set |
08714729789352 | Ureteral Stent Set |
08714729789345 | Ureteral Stent Set |
08714729789338 | Ureteral Stent Set |
08714729789321 | Ureteral Stent Set |
08714729789314 | Ureteral Stent Set |
08714729789307 | Ureteral Stent Set |
08714729789291 | Ureteral Stent Set |
08714729789284 | Ureteral Stent Set |
08714729789277 | Ureteral Stent Set |
08714729789260 | Ureteral Stent Set |
08714729789246 | Ureteral Stent Set |
08714729789239 | Ureteral Stent Set |
08714729462200 | Ureteral Stent Set |
08714729462538 | Ureteral Stent Set |
08714729462521 | Ureteral Stent Set |
08714729462392 | Ureteral Stent Set |
08714729462385 | Ureteral Stent Set |
08714729462323 | Ureteral Stent Set |
08714729462132 | Ureteral Stent Set |
08714729424239 | Ureteral Stent Set |
08714729424093 | Ureteral Stent Set |
08714729789451 | Ureteral Stent Set |