Swift Coil System

GUDID 00815948029651

SwiftPAC Coil, 9 cm

PENUMBRA, INC.

Non-neurovascular embolization coil
Primary Device ID00815948029651
NIH Device Record Keyc537c876-4a4c-423b-90ee-d1891817ba16
Commercial Distribution StatusIn Commercial Distribution
Brand NameSwift Coil System
Version Model Number400SWPC09-A
Company DUNS191077671
Company NamePENUMBRA, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Conditional
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100815948029651 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HCGDEVICE, NEUROVASCULAR EMBOLIZATION

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-24
Device Publish Date2024-04-16

On-Brand Devices [Swift Coil System]

00815948029736Swift Coil Detachment Handle
00815948029729SwiftPAC Coil, 55 cm
00815948029712SwiftPAC Coil, 50 cm
00815948029705SwiftPAC Coil, 40 cm
00815948029699SwiftPAC Coil, 35 cm
00815948029682SwiftPAC Coil, 25 cm
00815948029675SwiftPAC Coil, 20 cm
00815948029668SwiftPAC Coil, 12 cm
00815948029651SwiftPAC Coil, 9 cm
00815948029644SwiftPAC Coil, 2 cm
00815948029637SwiftPAC Coil, 1 cm
00815948029583SwiftPAC Coil, 60 cm
00815948029576SwiftPAC Coil, 45 cm
00815948029569SwiftPAC Coil, 30 cm
00815948029552SwiftPAC Coil, 15 cm
00815948029545SwiftPAC Coil, 10 cm
00815948029538SwiftPAC Coil, 8 cm
00815948029521SwiftPAC Coil, 7 cm
00815948029514SwiftPAC Coil, 6 cm
00815948029507SwiftPAC Coil, 5 cm
00815948024793SwiftPAC Coil, 4 cm
00815948024779SwiftPAC Coil, 3 cm

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.