SKIN PROTECTOR 1280

GUDID 00887868000324

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868000324
• NIH Device Record Key: ab323c2c-0e60-46cc-b244-c12cf1f38d48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SKIN PROTECTOR
• Version Model Number: 1280
• Catalog Number: 1280
• 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: false
• 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	00887868000324 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887868000324]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-11-22
• Device Publish Date: 2017-04-07

Devices Manufactured by Biomet Orthopedics, LLC

• 00880304009615 - BMP CABLE CUTTER: 2026-02-11
• 00880304387676 - OPEN END CUTTER: 2026-02-11
• 00887868000027 - TWIST DRILL BIT: 2026-02-11
• 00887868000645 - CALIBRATED TWIST DRILL: 2026-02-11
• 00887868048265 - EASYOUT: 2026-02-11
• 00887868048319 - EXTRACTION BOLT: 2026-02-11
• 00887868048326 - EXTRACTION BOLT: 2026-02-11
• 00887868048333 - EXTRACTION BOLT: 2026-02-11