Pulse Scientific Inc.

GUDID 00628055726012

Pulse Scientific Inc

Treponema pallidum reagin antibody IVD, kit, agglutination

• Primary Device ID: 00628055726012
• NIH Device Record Key: d844f916-a521-4423-b9bc-4ea4989a1299
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pulse Scientific Inc.
• Version Model Number: 10605
• Company DUNS: 249257254
• Company Name: Pulse Scientific Inc
• 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: true
• Manufacturing Date: false
• 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	00628055726012 [Primary]

FDA Product Code

• GMQ: Antigens, Nontreponemal, All

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: 2016-11-04

On-Brand Devices [Pulse Scientific Inc.]

• 00628055726036: 10503
• 00628055726029: 10103
• 00628055726012: 10605
• 00628055726005: 10603