Primary Device ID | 20705032056660 |
NIH Device Record Key | 26ad1c15-edcd-4c17-b0cd-49ecbecfe93c |
Commercial Distribution Discontinuation | 2024-06-18 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | ATW |
Version Model Number | 595MX014 |
Catalog Number | 595MX014 |
Company DUNS | 806136177 |
Company Name | CORDIS 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 | 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 | 10705032056663 [Primary] |
GS1 | 20705032056660 [Package] Contains: 10705032056663 Package: Box [1 Units] Discontinued: 2024-06-18 Not in Commercial Distribution |
DQX | Wire, guide, catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-26 |
Device Publish Date | 2024-06-18 |
20705032055212 - EMERALD | 2024-08-08 EMERALD GUIDEWIRES (OEM) |
20705032057407 - Palmaz Genesis | 2024-08-08 STENT GENESIS 12MM PERIPHERAL |
20705032057445 - Palmaz Genesis | 2024-08-08 STENT GENESIS 18MM PERIPHERAL |
20705032057537 - Palmaz Genesis | 2024-08-08 STENT GENESIS 29MM PERIPHERAL |
20705032057575 - Palmaz Genesis | 2024-08-08 STENT GENESIS 39MM PERIPHERAL |
20705032057612 - Palmaz Genesis | 2024-08-08 STENT GENESIS 59MM PERIPHERAL |
20705032062029 - PALMAZ BLUE | 2024-08-08 Blue/AviatorPlus 5x12/80P PKG |
20705032062258 - PALMAZ BLUE | 2024-08-08 Blue/AviatorPlus 5x24/80P PKG |