Philips Avent

GUDID 00075020070074

SCF332/21 F-Box

Philips Consumer Lifestyle B.V.

Breast pump, electric

• Primary Device ID: 00075020070074
• NIH Device Record Key: 69cae5fc-6c63-4165-80c1-a69c980cb9b9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Philips Avent
• Version Model Number: SCF332
• Company DUNS: 491996556
• Company Name: Philips Consumer Lifestyle B.V.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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	00075020070074 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K161532

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: 2017-09-17

On-Brand Devices [Philips Avent]

• 00075020070111: SCF334/26 F-Box
• 00075020070104: SCF334/25 F-Box
• 00075020070098: SCF334/23 F-Box
• 00075020070081: SCF334/22 F-Box
• 00075020070074: SCF332/21 F-Box
• 00075020107756: ME motor unit Qty: 1 - 2k expression kit (Body) Qty: 2 - Nat 3.0 bottle Qt:2 - Teat Qty:1 -