LOCATOR ABUTMENT PRE/KOH TG 2089

GUDID 00840481117848

LOCATOR ABUTMENT PRE/KOH TG MEDIUM PLATFORM, H. 2 MM

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00840481117848
• NIH Device Record Key: 8c02f3c2-6d88-418a-82dc-67961c6fb803
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOCATOR ABUTMENT PRE/KOH TG
• Version Model Number: 2089
• Catalog Number: 2089
• 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
GS1	00840481117848 [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

[00840481117848]

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: 2016-08-05

On-Brand Devices [LOCATOR ABUTMENT PRE/KOH TG]

• 00840481117848: LOCATOR ABUTMENT PRE/KOH TG MEDIUM PLATFORM, H. 2 MM
• 00840481117831: LOCATOR ABUTMENT PRE/KOH TG MEDIUM PLATFORM, H. 1 MM
• 00840481117824: LOCATOR ABUTMENT PRE/KOH TG MEDIUM PLATFORM, H. 0.2 MM
• 00840481117770: LOCATOR ABUTMENT PRE/KOH TG WIDE PLATFORM, H.2 MM
• 00840481117763: LOCATOR ABUTMENT PRE/KOH TG MEDIUM PLATFORM, H. 1.25 MM