MICRO ELITE 8301

GUDID 30841156101484

Micro Elite Snare 4mm

TELEFLEX INCORPORATED

Intravascular catheter-snare

• Primary Device ID: 30841156101484
• NIH Device Record Key: 6f7e6cb1-5fe3-4cf4-b87c-b2ca278c315d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MICRO ELITE
• Version Model Number: IPN913611
• Catalog Number: 8301
• 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
• 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
• 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: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter
• Width: 4 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841156101480 [Primary]
GS1	30841156101484 [Package]; Contains: 10841156101480; Package: Box [1 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K070502

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: 2
• Public Version Date: 2019-11-11
• Device Publish Date: 2019-06-11

On-Brand Devices [MICRO ELITE]

• 30841156101491: Micro Elite Snare 7mm
• 30841156101484: Micro Elite Snare 4mm
• 30841156101477: Micro Elite Snare 2mm