WALTERLORENZ™ SURGICAL ASSIST ARM WAL121

GUDID 00841036242169

BIOMET MICROFIXATION, INC

Medical equipment drape, single-use

• Primary Device ID: 00841036242169
• NIH Device Record Key: 2e72af81-d389-4376-99ec-6d9c5e9cce5e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: WALTERLORENZ™ SURGICAL ASSIST ARM
• Version Model Number: WAL121
• Catalog Number: WAL121
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036242169 [Primary]

FDA Product Code

• PUI: Drape, surgical, exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-02-06
• Device Publish Date: 2019-06-17

On-Brand Devices [WALTERLORENZ™ SURGICAL ASSIST ARM]

• 00841036242169: WAL121
• 00841036240790: WAL409
• 00841036240608: WAL405
• 00841036240592: WAL404
• 00841036240585: WAL407
• 00841036240578: WAL406
• 00841036240561: WAL403
• 00841036240554: WAL402
• 00841036240547: WAL401
• 00841036240530: WAL317
• 00841036240523: WAL316
• 00841036240516: WAL313
• 00841036240509: WAL311
• 00841036240493: WAL310
• 00841036240455: WAL306
• 00841036240448: WAL305
• 00841036240431: WAL304
• 00841036240424: WAL302
• 00841036240417: WAL301
• 00841036240400: WAL119
• 00841036240356: WAL100