MSOFT Dental Planning System

GUDID 07629999054356

Swissmeda AG

Dental treatment application software

• Primary Device ID: 07629999054356
• NIH Device Record Key: 09897471-76d2-48d8-8579-43a32fd30f13
• Commercial Distribution Discontinuation: 2020-01-17
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: MSOFT Dental Planning System
• Version Model Number: 2.14.3
• Company DUNS: 485199660
• Company Name: Swissmeda AG
• 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: 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 Identifiers

Device Issuing Agency	Device ID
GS1	07629999054356 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K112251

FDA Product Code

• LLZ: System, Image Processing, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-23
• Device Publish Date: 2019-02-15

On-Brand Devices [MSOFT Dental Planning System]

• 07629999054356: 2.14.3
• 07629999685093: 2.16
• 07629999628410: 2.19.0
• 07649997938021: MSOFT Dental Planning System