Dalbo®-PLUS / Dalbo® Classic 055647

GUDID 07640166514152

Dalbo®-PLUS / Dalbo® Classic Male part V

Cendres+Métaux SA

Dental anchor

• Primary Device ID: 07640166514152
• NIH Device Record Key: 1a3f0352-3c77-45ac-aa10-e571833b161d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Dalbo®-PLUS / Dalbo® Classic
• Version Model Number: 055647
• Catalog Number: 055647
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640166514152 [Primary]

FDA Product Code

• EJX: Anchor, Preformed

Sterilization

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

[07640166514152]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-14
• Device Publish Date: 2020-01-06

On-Brand Devices [Dalbo®-PLUS / Dalbo® Classic]

• 07640166514947: Dalbo®-PLUS / Dalbo® Classic Special parallelometer insert
• 07640166514152: Dalbo®-PLUS / Dalbo® Classic Male part V