Laguna Sand SBF 230V 412125

GUDID 00667259000573

Silhouet-Tone Corporation

General examination/treatment chair, electric General examination/treatment chair, electric

• Primary Device ID: 00667259000573
• NIH Device Record Key: 8a71557f-d01e-4122-8810-bbc497bcffde
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Laguna Sand SBF 230V
• Version Model Number: 412125
• Catalog Number: 412125
• Company DUNS: 242049828
• Company Name: Silhouet-Tone Corporation
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 450-687-9456
• Email: blapointe@silhouettone.com
• Phone: 450-687-9456
• Email: blapointe@silhouettone.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00667259000160 [Primary]
GS1	00667259000573 [Package]; Contains: 00667259000160; Package: skid [1 Units]; In Commercial Distribution

FDA Product Code

• LGX: Table, Examination, Medical, Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-08-14
• Device Publish Date: 2017-07-18

On-Brand Devices [Laguna Sand SBF 230V]

• 00667259000597: 412127
• 00667259000573: 412125