BIOARCH ST2008

GUDID 00889797053259

Trial Sizer

WRIGHT MEDICAL TECHNOLOGY, INC.

Surgical implant template, reusable

• Primary Device ID: 00889797053259
• NIH Device Record Key: 5b7910e4-fe40-4f40-91d8-e20d2a2edb95
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BIOARCH
• Version Model Number: ST2008
• Catalog Number: ST2008
• 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	00889797053259 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

Moist Heat or Steam Sterilization

[00889797053259]

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 [BIOARCH]

• 00889797053242: ST1030
• 00840420128928: ST1112
• 00840420128911: ST1111
• 00840420128904: ST1110
• 00840420128898: ST1109
• 00840420128881: ST1108
• 00889797053228: Insertion Driver Subtalar System
• 00889797055482: Subtalar Implant Alignment Rod
• 00889797055475: Alignment Rod
• 00889797053235: Probe Subtalar System
• 00889797053297: Trial Sizer
• 00889797053280: Trial Sizer
• 00889797053273: Trial Sizer
• 00889797053266: Trial Sizer
• 00889797053259: Trial Sizer