Swish™ Ball Abutment 9037-71

GUDID 10841307115632

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 10841307115632
• NIH Device Record Key: 87b21faf-6bcc-43c9-aa05-14cfe1203467
• Commercial Distribution Discontinuation: 2019-05-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Swish™ Ball Abutment
• Version Model Number: 9037-71
• Catalog Number: 9037-71
• Company DUNS: 868856969
• Company Name: IMPLANT DIRECT SYBRON MANUFACTURING LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: 1-888-649-6425
• Email: customerservice@implantdirect.com

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841307115632 [Primary]

Sterilization

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

[10841307115632]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 6
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-09-14

On-Brand Devices [Swish™ Ball Abutment]

• 10841307115724: 9048-75
• 10841307115717: 9048-74
• 10841307115700: 9048-73
• 10841307115694: 9048-72
• 10841307115687: 9048-71
• 10841307115670: 9037-75
• 10841307115663: 9037-74
• 10841307115656: 9037-73
• 10841307115649: 9037-72
• 10841307115632: 9037-71