Adlite™ II 354BKQ

GUDID 00634782572877

ADLITE II Penlight,Black, Disp pkg

AMERICAN DIAGNOSTIC CORP

Hand-held examination/treatment light

• Primary Device ID: 00634782572877
• NIH Device Record Key: 68aca29f-31be-4678-b56f-08d9ddfe24ff
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Adlite™ II
• Version Model Number: 354BKQ
• Catalog Number: 354BKQ
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 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	00634782073244 [Primary]
GS1	00634782572877 [Package]; Contains: 00634782872878; Package: Master Case [4 Units]; In Commercial Distribution
GS1	00634782872878 [Package]; Contains: 00634782073244; Package: Inner pack [12 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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

On-Brand Devices [Adlite™ II]

• 00634782572877: ADLITE II Penlight,Black, Disp pkg
• 00634782572495: ADLITE II Penlight,Black
• 00634782562021: ADLITE II Penlight, 18/cyl,White
• 00634782520984: ADLITE II Penlight,White, Disp pkg
• 00634782501754: ADLITE II Penlight,White