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
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• Phone: +1(800)255-2500
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• Phone: +1(800)255-2500
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• Phone: +1(800)255-2500
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• 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
• 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

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• 10705034219325 - EXPEDIUM: 2026-02-09 EXPEDIUM ANTERIOR SPINE SYSTEM DUAL HOLE STAPLE IMPACTOR
• 10705034219332 - EXPEDIUM: 2026-02-09 EXPEDIUM ANTERIOR SPINE SYSTEM FINISHING IMPACTOR, MODULAR
• 10705034467368 - EXPEDIUM: 2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER, CAP
• 10705034467375 - EXPEDIUM: 2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER, BODY
• 10705034467382 - EXPEDIUM: 2026-02-09 EXPEDIUM SPINE SYSTEM TAB BREAKER ASSEMBLY
• 10705034647074 - TELIGEN: 2025-12-18 TELIGEN Dilator Large
• 10705034647081 - TELIGEN: 2025-12-18 TELIGEN Dilator Medium