Indigo

GUDID 00815948022423

Indigo CATD Kit

PENUMBRA, INC.

Thrombectomy suction catheter

• Primary Device ID: 00815948022423
• NIH Device Record Key: 0f4dd92a-295b-45ca-97f2-78c596b09b77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Indigo
• Version Model Number: CATD-D
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00815948022423 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192833

FDA Product Code

• QEW: Peripheral Mechanical Thrombectomy With Aspiration

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: 2020-03-12
• Device Publish Date: 2020-03-04

On-Brand Devices [Indigo]

• 00814548017624: CATD
• 00814548017600: SEPD
• 00815948020481: Indigo CATD Kit
• 00815948022423: Indigo CATD Kit
• 00815948022348: Aspiration Catheter D Kit
• 00815948022331: Aspiration Catheter D Kit, CE
• 00814548019765: Ind Engine Canister Assembly, CE
• 00815948024281: Indigo CATD Kit