AM AM330002

GUDID 00889797043281

Plantar Cannula

WRIGHT MEDICAL TECHNOLOGY, INC.

Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable Orthopaedic implantation sleeve, reusable

• Primary Device ID: 00889797043281
• NIH Device Record Key: dc052d80-5470-49c1-9894-e8dfe4b5c4e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AM
• Version Model Number: AM330002
• Catalog Number: AM330002
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00889797043281 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

[00889797043281]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-08-11
• Device Publish Date: 2016-09-17

On-Brand Devices [AM]

• 00840420193001: AM96BLD5
• 00840420192943: AM96BLD1
• 00889797043618: AMCE9606
• 00889797043595: AMCE9603
• 00889797043540: AMCE3306
• 00889797043519: AMCE3303
• 00889797043458: AM960006
• 00889797043434: AM960003
• 00889797043601: Locking Attachment
• 00889797043588: Gastroc Cannula
• 00889797043571: Gastroc Obturator
• 00889797043533: Plantar Stop Device
• 00889797043502: Plantar Cannula
• 00889797043496: Plantar Obturator
• 00889797043441: Locking Attachment
• 00889797043427: Gastroc Cannula
• 00889797043410: Gastroc Obturator
• 00889797043281: Plantar Cannula
• 00889797043274: Plantar Obturator
• 00889797043526: Plantar Depth Gauge
• 00889797043304: Plantar Depth Gauge