Primary Device ID | 08714729847946 |
NIH Device Record Key | 7875534c-00a0-4a59-ab1b-42ef9ea7b308 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IntellaTip MiFi™ Reference Cable |
Version Model Number | M00436360 |
Catalog Number | M00436360 |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729847946 [Primary] |
OAD | catheter, percutaneous, cardiac ablation, for treatment of atrial flutter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2023-10-19 |
Device Publish Date | 2014-09-24 |
00191506046330 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046347 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046354 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046361 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046378 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046385 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046392 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
00191506046408 - Sterling™ | 2025-03-31 PTA Balloon Dilatation Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() INTELLATIP MIFI 97054414 not registered Live/Pending |
Boston Scientific Scimed, Inc. 2021-09-30 |