nfant® Patient Database ND3

GUDID 00861410000208

NFANT LABS LLC

Biofeedback system application software

• Primary Device ID: 00861410000208
• NIH Device Record Key: 3fa23b08-24e6-429b-bc6e-70475482c08c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: nfant® Patient Database
• Version Model Number: 1
• Catalog Number: ND3
• Company DUNS: 080007197
• Company Name: NFANT LABS LLC
• 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: false
• 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: false

Customer Support Contacts

• Phone: 1-800-761-7601
• Email: info@nfant.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00861410000208 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K143507

FDA Product Code

• HCC: Device, Biofeedback

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

Devices Manufactured by NFANT LABS LLC

• 00196852268917 - nfant® Thrive Feeding System: 2023-03-29
• 00861410000208 - nfant® Patient Database: 2018-07-06
• 00861410000208 - nfant® Patient Database: 2018-07-06
• 00861410000215 - nfant® SSB Sensor: 2018-07-06
• 00861410000239 - nfant® Coupling: 2018-07-06
• 00861410000246 - nfant® Mobile App: 2018-07-06