LOCATOR ABUTMENT PRE/KOH 3.30 1671

GUDID 00840481117305

LOCATOR ABUTMENT PRE/KOH 3.30 H.2 MM

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed

• Primary Device ID: 00840481117305
• NIH Device Record Key: 8d456dab-23cd-4f52-ac4d-986a850bb1aa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LOCATOR ABUTMENT PRE/KOH 3.30
• Version Model Number: 1671
• Catalog Number: 1671
• 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	00840481117305 [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

[00840481117305]

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 3.30]

• 00840481117312: LOCATOR ABUTMENT PRE/KOH 3.30 H.3 MM
• 00840481117305: LOCATOR ABUTMENT PRE/KOH 3.30 H.2 MM
• 00840481117299: LOCATOR ABUTMENT PRE/KOH 3.30 H.1 MM