DRILL GUIDE 214129400

GUDID 00887868446382

Biomet Orthopedics, LLC

Surgical drill guide, reusable

• Primary Device ID: 00887868446382
• NIH Device Record Key: 1b675ba0-7b70-4230-96ee-bfa783cf6b5a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRILL GUIDE
• Version Model Number: 2141-29-400
• Catalog Number: 214129400
• 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
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com
• Phone: +1(800)348-9500
• Email: customerservice@zimmerbiomet.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868446382 [Primary]

FDA Product Code

• FZX: Guide, surgical, instrument

Sterilization

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

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

[00887868446382]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-09-14
• Device Publish Date: 2020-09-04

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