LMH 62001013

GUDID 00889797025652

WRIGHT MEDICAL TECHNOLOGY, INC.

Surgical implant template, reusable

• Primary Device ID: 00889797025652
• NIH Device Record Key: a1c96312-b174-472c-a2eb-7418f58c6538
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LMH
• Version Model Number: 62001013
• Catalog Number: 62001013
• Company DUNS: 807201207
• Company Name: WRIGHT MEDICAL TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00889797025652 [Primary]

FDA Product Code

• KWD: PROSTHESIS, TOE, HEMI-, PHALANGEAL

Sterilization

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

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

[00889797025652]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2022-05-16
• Device Publish Date: 2016-09-17

On-Brand Devices [LMH]

• 00840420172211: 62101003
• 00840420172204: 62101002
• 00840420172198: 62101001
• 00840420168054: LMH-0003
• 00840420168047: LMH-0002
• 00840420168030: LMH-0001
• 00889797025607: 62001000
• 00889797025683: 62001023
• 00889797025676: 62001022
• 00889797025669: 62001021
• 00889797025652: 62001013
• 00889797025645: 62001012
• 00889797025638: 62001011
• 00889797025621: Impactor
• 00889797025614: Broach