Silverstein

GUDID 20681490040758

PACKING 1425015 6PK LONG STRIPS FLPL

MEDTRONIC XOMED, INC.

Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material Polyethylene craniofacial tissue reconstructive material

• Primary Device ID: 20681490040758
• NIH Device Record Key: 531b7823-4320-4f53-a336-b9cab936748a
• Commercial Distribution Discontinuation: 2018-12-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Silverstein
• Version Model Number: 1425015
• Company DUNS: 835465063
• Company Name: MEDTRONIC XOMED, INC.
• 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: 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

Device Dimensions

• Width: 31.2 Millimeter
• Width: 31.2 Millimeter
• Width: 31.2 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter
• Length: 6.4 Millimeter
• Width: 31.2 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00681490040754 [Primary]
GS1	20681490040758 [Package]; Contains: 00681490040754; Package: PK [6 Units]; Discontinued: 2018-12-20; Not in Commercial Distribution

FDA Product Code

• NOK: MATERIAL, EXTERNAL AESTHETIC RESTORATION, NO ADHESIVE

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: 2019-02-15
• Device Publish Date: 2017-10-13

On-Brand Devices [Silverstein]

• 20681490040819: PACKING 1428010 6PK REG STRIPS POLYEST
• 20681490040802: PACKING 1428005 6PK LONG STRIPS POLYEST
• 20681490040765: PACKING 1425020 6PK REG STRIPS FLPL
• 20681490040758: PACKING 1425015 6PK LONG STRIPS FLPL
• 00681490033428: PROSTHESIS 1112120 H/A INCUS-STAPES CONN
• 20681490030049: VENT TUBE 1028070 5PK SPAT 1.14X7MM SIL
• 20681490030032: VENT TUBE 1028065 5PK SPAT 1.14X12MM SIL
• 20763000038995: VENT TUBE 1028065 5PK SPAT 1.14X12MM SIL
• 00763000034757: PROSTHESIS 1112120 H/A INCUS-STAPES CONN