PMMA CAST.SLEEVE FOR RED. PAD PADR-CC

GUDID D7701589853

PMMA CAST.SLEEVE FOR RED. PAD NOT INDEXED

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7701589853
• NIH Device Record Key: 3e51aea9-edf3-4b52-8136-f9a2a5875630
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PMMA CAST.SLEEVE FOR RED. PAD
• Version Model Number: PADR-CC
• Catalog Number: PADR-CC
• 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	D7701589853 [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

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

[D7701589853]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-30
• Device Publish Date: 2022-03-22

On-Brand Devices [PMMA CAST.SLEEVE FOR RED. PAD]

• D7701589933: PMMA CAST.SLEEVE FOR RED. PAD TO CEMENT ON TITANIUM SLEEVES
• D7701589853: PMMA CAST.SLEEVE FOR RED. PAD NOT INDEXED