NEODENT 108.242

GUDID 04251574865137

Scanbody BASE

MEDENTiKA GmbH

Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning Dental implant abutment analog, scanning

• Primary Device ID: 04251574865137
• NIH Device Record Key: 96686639-c063-4fad-8cd0-cf22a5afa079
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NEODENT
• Version Model Number: 108.242
• Catalog Number: 108.242
• Company DUNS: 537555497
• Company Name: MEDENTiKA GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04251574865137 [Primary]

FDA Product Code

• NDP: Accessories, implant, dental, endosseous

Sterilization

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

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

[04251574865137]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-18
• Device Publish Date: 2024-03-08

On-Brand Devices [NEODENT]

• 04251574864888: Scanbody RevEX
• 04251574865137: Scanbody BASE