First Response™ Pregnancy Triple Check Pregnancy Test Kit

GUDID 00061700900700

FR-Early Result, Digital (Gold), Rapid Results

CHURCH & DWIGHT CO., INC.

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• Primary Device ID: 00061700900700
• NIH Device Record Key: efbbf763-e172-416d-9ffd-f4801c89af13
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: First Response™ Pregnancy Triple Check Pregnancy Test Kit
• Version Model Number: 00061700900700
• Company DUNS: 001211952
• Company Name: CHURCH & DWIGHT CO., 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: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: true

Customer Support Contacts

• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com
• Phone: +1(800)833-9532
• Email: Consumer.Relations@churchdwight.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00061700900700 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K123436

FDA Product Code

• LCX: KIT, TEST, PREGNANCY, HCG, OVER THE COUNTER

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: 2019-03-11
• Device Publish Date: 2019-02-19

On-Brand Devices [First Response™ Pregnancy Triple Check Pregnancy Test Kit]

• 00061700900700: FR-Early Result, Digital (Gold), Rapid Results
• 80022600020208: 00022600020202