EXPRO ELITE 8400

GUDID 30841156101507

Expro Elite Snare V1 5mm

TELEFLEX INCORPORATED

Intravascular catheter-snare

• Primary Device ID: 30841156101507
• NIH Device Record Key: c938510d-4787-4036-93d2-26cbd70fdc00
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EXPRO ELITE
• Version Model Number: IPN913613
• Catalog Number: 8400
• Company DUNS: 002348191
• Company Name: TELEFLEX INCORPORATED
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM
• Phone: +1(919)544-8000
• Email: CS@TELEFLEX.COM

Device Dimensions

• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter
• Width: 15 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156101503 [Primary]
GS1	30841156101507 [Package]; Contains: 10841156101503; Package: Box [1 Units]; Discontinued: 2019-06-19; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071457

FDA Product Code

• MMX: Device, percutaneous retrieval

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: 2019-11-11
• Device Publish Date: 2019-01-22

On-Brand Devices [EXPRO ELITE]

• 30841156101583: Expro Elite Snare V1 35mm
• 30841156101569: Expro Elite Snare V1 25mm
• 30841156101545: Expro Elite Snare V1 15mm
• 30841156101521: Expro Elite Snare V1 10mm
• 30841156101507: Expro Elite Snare V1 5mm
• 30841156101590: Expro Elite Snare V2 35mm
• 30841156101576: Expro Elite Snare V2 25mm
• 30841156101552: Expro Elite Snare V2 15mm
• 30841156101538: Expro Elite Snare V2 10mm
• 30841156101514: Expro Elite Snare V2 5mm