SELF HOLDING SCREW FORCEPS 939999262

GUDID 00887868067792

Biomet Orthopedics, LLC

Surgical implant handling forceps

• Primary Device ID: 00887868067792
• NIH Device Record Key: ca512160-8518-4078-a951-174d04fdd906
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SELF HOLDING SCREW FORCEPS
• Version Model Number: 939999262
• Catalog Number: 939999262
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887868067792 [Primary]

FDA Product Code

• HYA: FORCEPS, WIRE HOLDING

Sterilization

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

[00887868067792]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-27
• Device Publish Date: 2020-04-17

On-Brand Devices [SELF HOLDING SCREW FORCEPS]

• 00887868067792: 939999262
• 00887868446474: 939999262