Bailey Pappas

GUDID 00681490035859

PROSTHESIS 1156470 CUP PISTON .6X4.5 SST

MEDTRONIC XOMED, INC.

Ossicular prosthesis, partial

• Primary Device ID: 00681490035859
• NIH Device Record Key: 2bc66bb9-95dd-4f4b-b9f6-53a38b0881a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bailey Pappas
• Version Model Number: 1156470
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• 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
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Length: 4.5 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490035859 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K883727

FDA Product Code

• ETB: PROSTHESIS, PARTIAL OSSICULAR REPLACEMENT

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: 2018-07-06
• Device Publish Date: 2015-06-23

On-Brand Devices [Bailey Pappas]

• 00681490035859: PROSTHESIS 1156470 CUP PISTON .6X4.5 SST
• 00681490035842: PROSTHESIS 1156469 CUP PISTN .6X4.25 SST
• 00681490035835: PROSTHESIS 1156468 CUP PISTON .6X4 SST
• 00681490035828: PROSTHESIS 1156454 SST BUCKET .4X4.50
• 00681490035811: PROSTHESIS 1156453 SST BUCKET .4X4.25
• 00681490035804: PROSTHESIS 1156452 SST BUCKET .4X4.0