Paternity Test Kit 25

GUDID 10860013899285

Paternity Test Kit 25/cs

Ditek Consulting, LLC

Oral/upper respiratory tract specimen collection kit IVD, clinical

• Primary Device ID: 10860013899285
• NIH Device Record Key: ee790745-e8b2-4abd-bd17-e7e68fddd9c2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Paternity Test Kit 25
• Version Model Number: 92696
• Company DUNS: 111296701
• Company Name: Ditek Consulting, LLC
• 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: true
• Lot Batch: true
• Serial Number: false
• 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	00860013899288 [Primary]
GS1	10860013899285 [Package]; Contains: 00860013899288; Package: CASE [25 Units]; In Commercial Distribution

FDA Product Code

• NNK: Container, Specimen Mailer And Storage, Non-Sterile

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: 2025-05-14
• Device Publish Date: 2025-05-06

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