Primary Device ID | 20705032062258 |
NIH Device Record Key | ec084ffc-a347-49d4-b718-df23313b65c5 |
Commercial Distribution Discontinuation | 2024-07-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | PALMAZ BLUE |
Version Model Number | PB2450PPS |
Catalog Number | PB2450PPS |
Company DUNS | 806136177 |
Company Name | CORDIS CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 Issuing Agency | Device ID |
---|---|
GS1 | 10705032062251 [Primary] |
GS1 | 20705032062258 [Package] Contains: 10705032062251 Package: Box [1 Units] Discontinued: 2024-07-31 Not in Commercial Distribution |
FGE | Stents, drains and dilators for the biliary ducts |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-08 |
Device Publish Date | 2024-07-31 |
20705032062296 | Blue/AviatorPlus 7x24/80P PKG |
20705032062258 | Blue/AviatorPlus 5x24/80P PKG |
20705032062029 | Blue/AviatorPlus 5x12/80P PKG |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PALMAZ BLUE 76667477 3342464 Live/Registered |
CARDINAL HEALTH 529, LLC 2006-10-13 |