MDI 74001001

GUDID 00889797027472

Sizer

WRIGHT MEDICAL TECHNOLOGY, INC.

Surgical implant template, reusable

• Primary Device ID: 00889797027472
• NIH Device Record Key: d28ee8cf-e1a9-4c3c-ab3f-55a31b2d9113
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MDI
• Version Model Number: 74001001
• Catalog Number: 74001001
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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)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
• 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

• 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
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00889797027472 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

[00889797027472]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2022-08-16
• Device Publish Date: 2016-09-17

On-Brand Devices [MDI]

• 00840420195340: 10322
• 00840420173201: 74000004
• 00840420173195: 74000003
• 00840420173188: 74000002
• 00840420173171: 74000001
• 00840420150875: MD104
• 00840420150868: MD103
• 00840420150851: MD102
• 00840420150844: MD101
• 00889797027557: Impactor
• 00889797027458: Broach
• 00889797027441: Broach
• 00889797059619: Guide Pin
• 00889797059602: Olive Stabilizer
• 00889797059596: Guide Pin
• 00889797027625: Osteotomy Jig
• 00889797027618: Wire Guide
• 00889797027601: Osteotomy Jig
• 00889797027595: Osteotomy Jig
• 00889797027588: Wire Guide
• 00889797027571: Drill
• 00889797027564: Olive Wire
• 00889797027533: Drill
• 00889797027526: Broach Handle
• 00889797027519: QC Handle
• 00889797027465: Osteotomy Jig
• 00889797027502: Sizer
• 00889797027496: Sizer
• 00889797027489: Sizer
• 00889797027472: Sizer