Philips Avent Breast Pump

GUDID 00075020063830

SCF334/13

Philips Consumer Lifestyle B.V.

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• Primary Device ID: 00075020063830
• NIH Device Record Key: f112b7c6-6d23-49cb-865f-0dc38b4a23bb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Avent Breast Pump
• Version Model Number: SCF334
• Company DUNS: 491996556
• Company Name: Philips Consumer Lifestyle B.V.
• 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: true
• 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00075020063830 [Primary]

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-17

On-Brand Devices [Philips Avent Breast Pump]

• 00075020065803: SCF334
• 00075020063847: SCF334
• 00075020063830: SCF334/13
• 00075020060594: SCF334