Paternity Test Kit 1

GUDID 00860013899271

Paternity Test Kit 1 Single test

Ditek Consulting, LLC

Oral/upper respiratory tract specimen collection kit IVD, clinical

• Primary Device ID: 00860013899271
• NIH Device Record Key: e60a3121-f21e-4b5f-8188-b2f8e2dd67df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Paternity Test Kit 1
• Version Model Number: 96835
• 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	00860013899271 [Primary]

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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• 00860013969523 - Kidney Health Test Kit 3: 2025-05-14 These kits are designed to detect early signs of kidney damage or disease by analyzing your urine, blood, or both.
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