PRO-DENSE 12001500

GUDID 00889797998741

Guide Wire

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic implant calibration pin

• Primary Device ID: 00889797998741
• NIH Device Record Key: 13aae140-ac98-49da-82b6-1cb958b6d661
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO-DENSE
• Version Model Number: 12001500
• Catalog Number: 12001500
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, 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: true
• 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(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com
• Phone: +1(800)238-7117
• Email: customerservice@wmt.com

Device Dimensions

• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch
• Outer Diameter: 3.2 Millimeter
• Length: 11 Inch

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889797998741 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

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: 2022-08-15
• Device Publish Date: 2016-09-17

On-Brand Devices [PRO-DENSE]

• 00840420199546: 10001200
• 00840420171306: P7SM0404
• 00840420171290: P7SM0402
• 00840420159786: P7XS0404
• 00840420159731: 87XS0404
• 00840420159724: 87XS0402
• 00840420140791: 87SRIN04
• 00840420137302: 87SRCK15
• 00840420137296: 87SR0420
• 00840420137289: 87SR0410
• 00840420137272: 87SR0404
• 00840420128317: 12000400
• 00889797998765: 12001211
• 00889797998758: 12001216
• 00889797998727: 12001200
• 00889797998710: 12001208
• 00889797998703: 12001210
• 00889797998741: Guide Wire