RePlant® Multi-Unit Abutment 6060-61

GUDID 10841307126928

IMPLANT DIRECT SYBRON MANUFACTURING LLC

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 10841307126928
• NIH Device Record Key: 5b6eebc5-b74b-4e86-9113-4f3bf5f699cc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RePlant® Multi-Unit Abutment
• Version Model Number: 6060-61
• Catalog Number: 6060-61
• 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
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.com
• Phone: 1-888-649-6425
• Email: customerservice@implantdirect.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 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	10841307126928 [Primary]

Sterilization

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

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

[10841307126928]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-20
• Device Publish Date: 2021-04-12

On-Brand Devices [RePlant® Multi-Unit Abutment]

• 10841307126942: 6060-64
• 10841307126935: 6060-62
• 10841307126928: 6060-61
• 10841307126911: 6050-64
• 10841307126904: 6050-62
• 10841307126898: 6050-61
• 10841307126881: 6043-64
• 10841307126874: 6043-62
• 10841307126867: 6043-61
• 10841307126850: 6035-64
• 10841307126843: 6035-62