SWANSON II

GUDID 00840420198860

WRIGHT MEDICAL TECHNOLOGY, INC.

Surgical implant template, reusable

• Primary Device ID: 00840420198860
• NIH Device Record Key: e8158fb0-5698-4a56-8e31-4357ae1abec9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SWANSON II
• Version Model Number: 4980300
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840420198860 [Primary]

FDA Product Code

• KIG: PROSTHESIS, WRIST, CONSTRAINED, POLYMER

Sterilization

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

[00840420198860]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-26
• Device Publish Date: 2016-09-17

On-Brand Devices [SWANSON II]

• 00840420198860: 4980300
• 00840420130655: G4880305J
• 00840420130648: G4880304J
• 00840420130631: G4880303J
• 00840420130624: G4880302J
• 00840420130617: G4880301J