Advanced Double Electric Breast Pump

GUDID 00849409000019

Evenflo Feeding, Inc. Advanced Double Electric Breast Pump

EVENFLO FEEDING, INC.

Breast pump, electric

• Primary Device ID: 00849409000019
• NIH Device Record Key: 5d2d1935-72d6-4231-a99b-e209d8e19d1a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Advanced Double Electric Breast Pump
• Version Model Number: 2951
• Company DUNS: 078611319
• Company Name: EVENFLO FEEDING, 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: true
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00849409000019 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131153

FDA Product Code

• HGX: Pump, Breast, Powered

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: 2016-09-26

Devices Manufactured by EVENFLO FEEDING, INC.

• 00849409000019 - Advanced Double Electric Breast Pump: 2018-07-06Evenflo Feeding, Inc. Advanced Double Electric Breast Pump
• 00849409000019 - Advanced Double Electric Breast Pump: 2018-07-06 Evenflo Feeding, Inc. Advanced Double Electric Breast Pump
• 00849409000033 - Single Electric Breast Pump: 2018-07-06 Evenflo Feeding, Inc. Single Electric Breast Pump
• 00849409000040 - Advanced Single Electric Breast Pump: 2018-07-06 Evenflo Feeding, Inc. Advanced Double Electric Breast Pump