VAROGuide PreGuide

GUDID 08800038700055

DMS Co., Ltd.

Dental guided surgery reference plate Dental guided surgery reference plate Dental guided surgery reference plate Dental guided surgery reference plate Dental guided surgery reference plate Dental guided surgery reference plate Dental guided surgery reference plate

• Primary Device ID: 08800038700055
• NIH Device Record Key: ed04ea93-ca99-484b-96b5-118172f5915a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VAROGuide PreGuide
• Version Model Number: PGFL
• Company DUNS: 688444000
• Company Name: DMS Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: MR Safe
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800038700055 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-07-13
• Device Publish Date: 2022-07-05

On-Brand Devices [VAROGuide PreGuide]

• 08800038700109: PGUVRS
• 08800038700093: PGS24
• 08800038700086: PGS13
• 08800038700079: PGFS
• 08800038700062: PGFM
• 08800038700055: PGFL
• 08800038700048: PGA
• 08800038700031: PGM24
• 08800038700024: PGM13