MILLABLE POST, REP., EXTERNAL A-TG-MFE-W

GUDID D7700875803

MILLABLE POST, REP., EXTERNAL PROF., PRE-KOH TG, WIDE PLAT.

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: D7700875803
• NIH Device Record Key: e8a9c7a7-947c-479b-83a5-8ce7712b59b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MILLABLE POST, REP., EXTERNAL
• Version Model Number: A-TG-MFE-W
• Catalog Number: A-TG-MFE-W
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D7700875803 [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

[D7700875803]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-11-08
• Device Publish Date: 2015-10-01

On-Brand Devices [MILLABLE POST, REP., EXTERNAL]

• D7700875803: MILLABLE POST, REP., EXTERNAL PROF., PRE-KOH TG, WIDE PLAT.
• D7700875793: MILLABLE POST, REP., EXTERNAL PROF., PRE-KOH TG,MEDIUM PLAT.