Swish™ Straight Abutment 9037-21

GUDID 10841307116370

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 10841307116370
• NIH Device Record Key: a7541406-89e6-4a35-b92a-22ee7989933b
• Commercial Distribution Discontinuation: 2019-05-22
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Swish™ Straight Abutment
• Version Model Number: 9037-21
• Catalog Number: 9037-21
• 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	10841307116370 [Primary]

Sterilization

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

[10841307116370]

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™ Straight Abutment]

• 10841307116554: 9065-20
• 10841307116547: 9048-20
• 10841307116424: 9048-23
• 10841307116417: 9048-22
• 10841307116400: 9048-21
• 10841307116394: 9037-23
• 10841307116387: 9037-22
• 10841307116370: 9037-21