LACTOSORB* SYSTEM 915-2028

GUDID 00841036054045

BIOMET MICROFIXATION, INC

Bone tap, single-use, non-sterile

• Primary Device ID: 00841036054045
• NIH Device Record Key: 8c9a9ade-1caf-4049-90c9-36114d094ab2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LACTOSORB* SYSTEM
• Version Model Number: 915-2028
• Catalog Number: 915-2028
• 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	00841036054045 [Primary]

FDA Product Code

• HWX: TAP, BONE

Sterilization

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

[00841036054045]

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* SYSTEM]

• 00841036140953: 72-2000
• 00841036064419: 915-2016
• 00841036054168: 915-2047
• 00841036054144: 915-2040
• 00841036054106: 915-2035
• 00841036054045: 915-2028
• 00841036053956: 915-2014