ABUTMENT SCREW M1.8 SH-VABU180-200-6

GUDID D7701595423

ABUTMENT SCREW M1.8 -M.2 H.6 MM FOR XA

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7701595423
• NIH Device Record Key: 676cf2d3-03ee-4591-b52d-a9cada6fabbd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ABUTMENT SCREW M1.8
• Version Model Number: SH-VABU180-200-6
• Catalog Number: SH-VABU180-200-6
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7701595423 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162004

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

[D7701595423]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-02-23
• Device Publish Date: 2022-02-15

On-Brand Devices [ABUTMENT SCREW M1.8]

• D7701235203: ABUTMENT SCREW M1.8 CONICAL SUPPORT CONNECT.10 PCS
• D7701235193: ABUTMENT SCREW M1.8 CONICAL SUPPORT CONNECTION
• D7700640793: ABUTMENT SCREW M1.8 PRE-KOH D.3.30/3.80 MM
• D7701595423: ABUTMENT SCREW M1.8 -M.2 H.6 MM FOR XA
• D7701595413: ABUTMENT SCREW M1.8 -M.2 H.5 MM FOR XA
• D7701595403: ABUTMENT SCREW M1.8 -M.2 H.4 MM FOR XA