LACTOSORB* 2.0MM SYSTEM 915-2072

GUDID 00841036054274

BIOMET MICROFIXATION, INC

Bone tap, single-use, non-sterile

• Primary Device ID: 00841036054274
• NIH Device Record Key: 8bd74750-ebea-47f9-b453-a77a3d8b4b2f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LACTOSORB* 2.0MM SYSTEM
• Version Model Number: 915-2072
• Catalog Number: 915-2072
• Company DUNS: 046189866
• Company Name: BIOMET MICROFIXATION, INC
• 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(904)741-4400
• Email: FXJAX-ORDERS@ZIMMERBIOMET.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841036054274 [Primary]

FDA Product Code

• HWX: TAP, BONE

Sterilization

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

[00841036054274]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-15
• Device Publish Date: 2018-09-14

On-Brand Devices [LACTOSORB* 2.0MM SYSTEM]

• 00841036054298: 915-2074
• 00841036054274: 915-2072
• 00841036054250: 915-2070
• 00841036054038: 915-2027
• 00841036053949: 915-2011
• 00841036053918: 915-2003