CAST. NON REP. POST WITH CR-CO PADR-UCRCO

GUDID D7701589883

CAST. NON REP. POST WITH CR-CO BASE, RED. PAD ABUT.

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7701589883
• NIH Device Record Key: 911ef313-0c6c-4c3a-9e88-3dae77aabb47
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAST. NON REP. POST WITH CR-CO
• Version Model Number: PADR-UCRCO
• Catalog Number: PADR-UCRCO
• 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	D7701589883 [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

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

Moist Heat or Steam Sterilization

[D7701589883]

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 [CAST. NON REP. POST WITH CR-CO]

• D7701081903: CAST. NON REP. POST WITH CR-CO BASE, PAD ABUT.
• D7701589883: CAST. NON REP. POST WITH CR-CO BASE, RED. PAD ABUT.