CALIBRATED DRILL BIT 214113032

GUDID 00887868024184

Biomet Orthopedics, LLC

Fluted surgical drill bit, single-use, non-sterile

• Primary Device ID: 00887868024184
• NIH Device Record Key: f456d020-2a6f-42a9-9e69-c83569d8b397
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CALIBRATED DRILL BIT
• Version Model Number: 2141-13-032
• Catalog Number: 214113032
• 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: true
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868024184 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

[00887868024184]

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: 2017-04-25

On-Brand Devices [CALIBRATED DRILL BIT]

• 00880304491670: 27580
• 00887868024955: 2142-27-070
• 00887868024436: 2141-29-000
• 00887868024207: 2141-14-038
• 00887868024184: 2141-13-032
• 00887868045448: 8162-99-009
• 00887868447167: 8162-99-009
• 00887868446597: 2142-27-070