PRE-MADE STRAIGHT ABUT. FOR A-PLAIN-MDT-10

GUDID D7702472553

PRE-MADE STRAIGHT ABUT. FOR ANG ABUT. D3.30 H10MM NOT REP

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7702472553
• NIH Device Record Key: dbedf334-43ad-4a47-92e2-f967185ae6ac
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRE-MADE STRAIGHT ABUT. FOR
• Version Model Number: A-PLAIN-MDT-10
• Catalog Number: A-PLAIN-MDT-10
• 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
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com
• Phone: 844.862.7846
• Email: info.us@sweden-martina.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7702472553 [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

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

[D7702472553]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-05
• Device Publish Date: 2023-05-26

On-Brand Devices [PRE-MADE STRAIGHT ABUT. FOR]

• D7702472553: PRE-MADE STRAIGHT ABUT. FOR ANG ABUT. D3.30 H10MM NOT REP
• D7702472523: PRE-MADE STRAIGHT ABUT. FOR ANG ABUT. D3.30 H6MM NOT REP