CANNULATED CANCELLOUS TAP 246114634

GUDID 00887868027529

Biomet Orthopedics, LLC

Bone tap, single-use, sterile Bone tap, single-use Bone tap, single-use Bone tap, single-use Bone tap, single-use Bone tap, single-use Bone tap, single-use Bone tap, single-use Bone tap, single-use

• Primary Device ID: 00887868027529
• NIH Device Record Key: e923803f-b122-4405-8b58-1e96e1f9d008
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CANNULATED CANCELLOUS TAP
• Version Model Number: 2461-14-634
• Catalog Number: 246114634
• 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: true
• 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

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 Identifiers

Device Issuing Agency	Device ID
GS1	00887868027529 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-28

On-Brand Devices [CANNULATED CANCELLOUS TAP]

• 00887868027529: 2461-14-634
• 00887868024580: 2141-46-100
• 00887868024573: 2141-46-000
• 00887868002861: 14634
• 00887868001895: 13585
• 00887868446580: 13585
• 00887868458446: 2141-46-000
• 00887868027505: 2461-14-627