CERENOVUS EVT110

GUDID 10886704084563

CERENOVUS Aspiration Tubing Set ID: 0.110 in / 2.79 mm Working length: 112 in / 284 cm

Medos International Sàrl

Vascular guide-catheter, single-use

• Primary Device ID: 10886704084563
• NIH Device Record Key: 2150619b-ee28-40bc-98b7-39c47b763012
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CERENOVUS
• Version Model Number: EVT110
• Catalog Number: EVT110
• Company DUNS: 482661753
• Company Name: Medos International Sàrl
• 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: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886704084563 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K193380

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: 2021-05-24
• Device Publish Date: 2021-05-14

Devices Manufactured by Medos International Sàrl

• 10886705001163 - VERSALOK: 2025-05-08 Versalok Anchor with Threader Tab
• 10886705032952 - GRYPHON X: 2025-04-30 GRYPHON X PUSH-IN BR Anchor w/ DYNACORD and Needles
• 10886705032969 - GRYPHON X: 2025-04-30 GRYPHON X PUSH-IN BR Anchor_x000D_ w/ Dual Strand DYNACORD and Needles
• 10886705032976 - GRYPHON X: 2025-04-30 GRYPHON X THREADED BR Anchor_x000D_ w/ DYNACORD and Needles
• 10886705032983 - GRYPHON X: 2025-04-30 GRYPHON X THREADED BR Anchor _x000D_ w/ Dual Strand DYNACORD and Needles
• 10886705032990 - GRYPHON X: 2025-04-30 GRYPHON X PUSH-IN PEEK Anchor _x000D_ w/ DYNACORD and Needles
• 10886705033003 - GRYPHON X: 2025-04-30 GRYPHON X PUSH-IN PEEK Anchor _x000D_ w/ Dual Strand DYNACORD and Needles
• 10886705033010 - GRYPHON X: 2025-04-30 GRYPHON X PUSH-IN BR Anchor _x000D_ w/ 1.3mm PERMATAPE and Needles