NON REP. ABUTMENT H2.5 MM FOR E-ABUT-330-2.5

GUDID D7700610423

NON REP. ABUTMENT H2.5 MM FOR OUTLINK2 D.3.30/4.10SP

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7700610423
• NIH Device Record Key: 6b168803-070b-46dc-9df4-48fca28fdea8
• Commercial Distribution Discontinuation: 2015-10-13
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: NON REP. ABUTMENT H2.5 MM FOR
• Version Model Number: E-ABUT-330-2.5
• Catalog Number: E-ABUT-330-2.5
• Company DUNS: 433815198
• Company Name: SWEDEN & MARTINA SPA
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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: 844.862.7846
• Email: info.us@sweden-martina.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7700610423 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K142242

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[D7700610423]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-10-13

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