ALPS SSI003363

GUDID 00880304848498

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00880304848498
• NIH Device Record Key: 1ee4b802-8b7b-4aab-a66e-d2868d66412d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ALPS
• Version Model Number: SSI003363
• Catalog Number: SSI003363
• Company DUNS: 129278169
• Company Name: Biomet Orthopedics, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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) 343-9500
• Email: customerservice@zimmerbiomet.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304848498 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132898

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

[00880304848498]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-11-22
• Device Publish Date: 2018-09-12

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• 00887868571718 - RingLoc®+ Triflange: 2025-06-20
• 00887868571725 - RingLoc®+ Triflange: 2025-06-20
• 00887868571732 - RingLoc®+ Triflange: 2025-06-20
• 00887868571749 - RingLoc®+ Triflange: 2025-06-20
• 00887868571756 - RingLoc®+ Triflange: 2025-06-20
• 00887868571763 - RingLoc®+ Triflange: 2025-06-20