Metalite 353Q-3MC

GUDID 00634782595418

METALITE II Penlight,Assorted, Disp pkg, 3/pkg

AMERICAN DIAGNOSTIC CORP

Hand-held examination/treatment light Hand-held examination/treatment light

• Primary Device ID: 00634782595418
• NIH Device Record Key: 239a1f65-5d72-48a9-9000-d3330f457eb2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Metalite
• Version Model Number: 353Q-3MC
• Catalog Number: 353Q-3MC
• Company DUNS: 108999095
• Company Name: AMERICAN DIAGNOSTIC CORP
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 1-800-232-2670
• Email: info@adctoday.com
• Phone: 1-800-232-2670
• Email: info@adctoday.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00634782093990 [Primary]
GS1	00634782595418 [Package]; Contains: 00634782895419; Package: Master [16 Units]; In Commercial Distribution
GS1	00634782895419 [Package]; Contains: 00634782093990; Package: Inner [4 Units]; In Commercial Distribution

FDA Product Code

• KYT: Light, Examination, Medical, Battery Powered

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: 2018-09-03
• Device Publish Date: 2018-08-03

On-Brand Devices [Metalite]

• 00634782595418: METALITE II Penlight,Assorted, Disp pkg, 3/pkg
• 00634782595401: METALITE Penlightw/Pupil Gauge,White, Disp pkg, 3/pkg