JET 5MAXJETDKIT

GUDID 00814548019741

5MAXJETDKIT-A

PENUMBRA, INC.

Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter Thrombectomy suction catheter

• Primary Device ID: 00814548019741
• NIH Device Record Key: 0c5d330a-20b7-4df2-94fc-bd6550581514
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: JET
• Version Model Number: 5MAXJETDKIT-A
• Catalog Number: 5MAXJETDKIT
• Company DUNS: 191077671
• Company Name: PENUMBRA, INC.
• 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: 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00814548019741 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K113163

FDA Product Code

• NRY: CATHETER, THROMBUS RETRIEVER

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-09-24
• Device Publish Date: 2018-08-23

On-Brand Devices [JET]

• 00814548019802: 5MAXJETDKIT
• 00814548019796: 5MAXJETD
• 00814548019741: 5MAXJETDKIT-A
• 00814548019734: 5MAXJETD-A