Indigo

GUDID 00814548017624

PENUMBRA, INC.

Thrombectomy suction catheter

• Primary Device ID: 00814548017624
• NIH Device Record Key: b00255f6-0ab9-4707-ba70-939b70cdc652
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Indigo
• Version Model Number: CATD
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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	00814548017624 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142870

FDA Product Code

• DXE: Catheter, embolectomy

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-03-15

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