Primary Device ID | 20705032101049 |
NIH Device Record Key | 7ffbe066-b774-4b2a-b6b4-000b7b6beafa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BRITECROSS™ Support Catheter |
Version Model Number | BC14150 |
Catalog Number | BC14150 |
Company DUNS | 118274128 |
Company Name | Cordis US Corp. |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 20705032101049 [Primary] |
DQY | Catheter, Percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-09-09 |
Device Publish Date | 2025-09-01 |
20705032101124 | BriteCross .035 x 190CM |
20705032101117 | BriteCross .035 x 135CM |
20705032101100 | BriteCross .035 x 90CM |
20705032101094 | BriteCross .018 x 200CM |
20705032101087 | BriteCross .018 x 150CM |
20705032101070 | BriteCross .018 x 90CM |
20705032101063 | BriteCross .018 x 65CM |
20705032101056 | BriteCross .014 x 200CM |
20705032101049 | BriteCross .014 x 150CM |
20705032101032 | BriteCross .014 x 90CM |
20705032101025 | BriteCross .014 x 65CM |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BRITECROSS 98129268 not registered Live/Pending |
Cordis US Corp 2023-08-11 |