DRILL GUIDE 25015

GUDID 00887868073588

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868073588
• NIH Device Record Key: 3933e1b6-ffeb-4198-8410-0f58431e2df4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL GUIDE
• Version Model Number: 25-015
• Catalog Number: 25015
• 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	00887868073588 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00887868073588]

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: 2017-07-28

On-Brand Devices [DRILL GUIDE]

• 00887868109621: 110008428
• 00887868109607: 110008418
• 00887868109591: 110008413
• 00887868073588: 25-015
• 00887868070709: DG20
• 00887868024085: 2141-07-029
• 00887868000621: 1732
• 00887868109614: 110008423
• 00887868447266: 8162-99-012
• 00887868446436: 8241-64-070
• 00887868446382: 2141-29-400
• 00887868448652: DG20
• 00887868463167: 110008428
• 00887868463150: 110008423
• 00887868463143: 110008418
• 00887868463136: 110008413