PRE-MADE NON REP. POST FOR L-MD.-340-8-ROT

GUDID D7701827033

PRE-MADE NON REP. POST FOR PRAMA IMPLANT, D. 3.40 H.8 MM

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7701827033
• NIH Device Record Key: ca540917-f3c0-4277-a8e8-d46b4cde1679
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRE-MADE NON REP. POST FOR
• Version Model Number: L-MD.-340-8-ROT
• Catalog Number: L-MD.-340-8-ROT
• 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	D7701827033 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K180365

FDA Product Code

• NHA: Abutment, Implant, Dental, Endosseous

Sterilization

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

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

[D7701827033]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-03-02
• Device Publish Date: 2022-02-22

On-Brand Devices [PRE-MADE NON REP. POST FOR ]

• D7701284513: PRE-MADE NON REP. POST FOR PRAMA IMPLANT, D. 3.40 H.8 MM
• D7701284503: PRE-MADE NON REP. POST FOR PRAMA IMPLANT, D. 3.40 H.6 MM
• D7701422413: PRE-MADE NON REP. POST FOR ANGLED PROSTHESIS D.3.40 H.6MM
• D7701591773: PRE-MADE NON REP. POST FOR ANGLED PROSTHESIS D.3.40 H.10MM
• D7701827073: PRE-MADE NON REP. POST FOR ANGLED PROSTHESIS D.3.40 H.10MM
• D7701827033: PRE-MADE NON REP. POST FOR PRAMA IMPLANT, D. 3.40 H.8 MM
• D7701827023: PRE-MADE NON REP. POST FOR PRAMA IMPLANT, D. 3.40 H.6 MM
• D7701524783: PRE-MADE NON REP. POST FOR ANGLED PROSTHESIS D.3.40 H.6MM