Primary Device ID | 00815948029569 |
NIH Device Record Key | 868e9342-e53c-4475-bbdf-fda5a87171ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Swift Coil System |
Version Model Number | 400SWPC30-A |
Company DUNS | 191077671 |
Company Name | PENUMBRA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00815948029569 [Primary] |
HCG | DEVICE, NEUROVASCULAR EMBOLIZATION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-24 |
Device Publish Date | 2024-04-16 |
00815948029736 | Swift Coil Detachment Handle |
00815948029729 | SwiftPAC Coil, 55 cm |
00815948029712 | SwiftPAC Coil, 50 cm |
00815948029705 | SwiftPAC Coil, 40 cm |
00815948029699 | SwiftPAC Coil, 35 cm |
00815948029682 | SwiftPAC Coil, 25 cm |
00815948029675 | SwiftPAC Coil, 20 cm |
00815948029668 | SwiftPAC Coil, 12 cm |
00815948029651 | SwiftPAC Coil, 9 cm |
00815948029644 | SwiftPAC Coil, 2 cm |
00815948029637 | SwiftPAC Coil, 1 cm |
00815948029583 | SwiftPAC Coil, 60 cm |
00815948029576 | SwiftPAC Coil, 45 cm |
00815948029569 | SwiftPAC Coil, 30 cm |
00815948029552 | SwiftPAC Coil, 15 cm |
00815948029545 | SwiftPAC Coil, 10 cm |
00815948029538 | SwiftPAC Coil, 8 cm |
00815948029521 | SwiftPAC Coil, 7 cm |
00815948029514 | SwiftPAC Coil, 6 cm |
00815948029507 | SwiftPAC Coil, 5 cm |
00815948024793 | SwiftPAC Coil, 4 cm |
00815948024779 | SwiftPAC Coil, 3 cm |