N/A

GUDID 00763000571092

ACCY 3755-40 TUNNELNG TOOL DBS EMAN LL61

Covidien LP

Subcutaneous tunneller, single-use

• Primary Device ID: 00763000571092
• NIH Device Record Key: f8dfeca3-238f-4328-a73c-7a0c178910a9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N/A
• Version Model Number: 3755-40
• Company DUNS: 058614483
• Company Name: Covidien LP
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter
• Length: 40 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000571092 [Primary]

FDA Product Code

• HAO: INSTRUMENT, SURGICAL, NON-POWERED

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: 2022-06-13
• Device Publish Date: 2022-06-04

On-Brand Devices [N/A]

• 00821684074176: ATHERECTOMY FG02550 CUTTERDRIVER V04
• 00763000571092: ACCY 3755-40 TUNNELNG TOOL DBS EMAN LL61