CINCH MODULAR ATTACHMENTS 31-555618

GUDID 00880304468641

Biomet Orthopedics, LLC

Orthopaedic implant impactor

• Primary Device ID: 00880304468641
• NIH Device Record Key: 5f1b295e-c3ec-40fa-a119-cebd945c1ce4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CINCH MODULAR ATTACHMENTS
• Version Model Number: 31-555618
• Catalog Number: 31-555618
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• 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)348-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304468641 [Primary]

FDA Product Code

• HWA: IMPACTOR

Sterilization

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

[00880304468641]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [CINCH MODULAR ATTACHMENTS]

• 00880304468658: 31-555613
• 00880304468641: 31-555618
• 00880304468481: 31-555614
• 00880304464131: 31-555612
• 00880304608450: 31-555617
• 00880304608443: 31-555615
• 00887868482854: 31-555617
• 00887868482847: 31-555616
• 00887868482830: 31-555615
• 00887868482816: 31-555613
• 00887868482793: 31-555611
• 00887868482861: 31-555618
• 00887868482809: 31-555612