Dalbo®-Classic 055892

GUDID 07640173090953

Dalbo®-Classic EV elliptic

Cendres+Métaux SA

Dental anchor

• Primary Device ID: 07640173090953
• NIH Device Record Key: 800b0b68-3b20-488d-b343-4276eb3b383b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dalbo®-Classic
• Version Model Number: 055892
• Catalog Number: 055892
• Company DUNS: 487506230
• Company Name: Cendres+Métaux SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Manufacturing Date: true
• Expiration Date: false
• 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: +41583602000
• Email: info@cmsa.ch

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640173090953 [Primary]

FDA Product Code

• EGG: Attachment, Precision, All

Sterilization

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

[07640173090953]

Moist Heat or Steam Sterilization;High-level Disinfectant

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-08
• Device Publish Date: 2020-03-31

On-Brand Devices [Dalbo®-Classic]

• 07640173091264: Dalbo®-Classic Spacer G
• 07640173090960: Dalbo®-Classic EK elliptic
• 07640173090953: Dalbo®-Classic EV elliptic
• 07640173090946: Dalbo®-Classic Female part E elliptic
• 07640173090915: Dalbo®-Classic Female part E basic
• 07640173090106: Dalbo®-Classic EK basic
• 07640173090090: Dalbo®-Classic EV basic
• 07640173090892: Dalbo®-Classic Elastomeric ring