Primary Device ID | 00884838059269 |
NIH Device Record Key | 75cf20f0-4683-4684-b4e9-917154fc5597 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | StentBoost |
Version Model Number | StentBoost R4 |
Catalog Number | 001007 |
Company DUNS | 413819707 |
Company Name | Philips Medical Systems Nederland B.V. |
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 | false |
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 | 00884838059269 [Primary] |
OWB | Interventional Fluoroscopic X-Ray System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 8 |
Public Version Date | 2019-12-02 |
Device Publish Date | 2016-09-24 |
00884838118454 - Philips | 2024-07-26 MRI Needle Block 8G |
00884838118461 - Philips | 2024-07-26 Fiducial Marker Sleeve Assembly |
00884838118478 - Philips | 2024-07-26 FIDUCIAL MARKER GRID BLOCK ASSEMBLY |
00884838118485 - Philips | 2024-07-26 MRI Needle Block 12G |
00884838118492 - Philips | 2024-07-26 MRI Needle Block 14G |
00884838118508 - Philips | 2024-07-26 MRI Needle Block 16G |
00884838118515 - Philips | 2024-07-26 MRI Needle Block 18G |
00884838118522 - Philips | 2024-07-26 MRI Needle Sleeve 12G |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
STENTBOOST 79002072 3029257 Live/Registered |
Koninklijke Philips N.V. 2004-03-31 |